549. âA Novel Tyrosine Hyperoxidation Enables Selective Peptide Cleavage,â S. Zhang, L. M. De Leon Rodriguez, F. F. Li, R. Huang, I. K. H. Leung, P. W. R. Harris and M. A. Brimble, Chemical Science, 2022, DOI: 10.1039/D1SC06216F. (IF = 9.8)
548. âLipidated Calcitonin Gene-related Peptide (CGRP) Peptide Antagonists Retain CGRP Receptor Activity and
Attenuate CGRP Action in vivo,â A. Jamaluddin, C.-L. Chuang, E. T. Williams, A. Siow, S. H. Yang, P. W. R. Harris, J. Petersen, R. L Bower, S. Chand, M. A. Brimble, C. S. Walker, D. L. Hay and K. M. Loomes, Frontiers in Pharmacology (Translational Pharmacology), 2022, in press. (IF = 5.8)
547. âNitrobenzoxadiazole Derivatives of the Rat Selective Toxicant Norbormide as Fluorescent Probes for Live Cell Imaging,â Z. L. Wang, F. F. Li, R. Quach, A. Ferrarese, A. Forgiarini, M. Ferrari, C. DâAmore, S. Bova, G. Orso, F. Fusi, S. Saponara, B. Hopkins, M. A. Brimble and D. Rennison, Bioorganic and Medicinal Chemistry, 2022, in press. (IF = 3.64)
546. âA Solid Support-based Synthetic Strategy for the Site-selective Functionalization of Peptides with Organometallic Half-sandwich Moieties,â D. Truong, N. Y. S. Lam, M. Kamalov, M. Riisom, S. M. F. Jamieson, P. W. R. Harris, M. A. Brimble, N. Metzler-Nolte and C. G. Hartinger, Chemistry – A European Journal, 2022, in press. (IF = 5.2)
545. âTowards Eco-friendly Marine Antifouling Biocides â Nature Inspired Tetrasubstituted 2,5-Diketopiperazines,â T. M. Grant, D. Rennison, G. Cervin, H. Pavia, C. Hellio, V. Foulon, M. A. Brimble, P. Cahill and J. Swenson, Science of the Total Environment, 2022, 812, 154287-154298. (IF = 7.96) (included in Special Issue: âWater Health and Ecosystem.â
544. âTotal Synthesis of Novel Antimicrobial β-Hairpin Capitellacin via Rapid Flow-Based SPPS Assembly
and Regioselective On-Resin Disulfide Cyclisation,â O. A. Shepperson, C. C. Hanna, M. A. Brimble, P. W. R. Harris and A. J. Cameron, International Journal of Peptide Research and Therapeutics, 2022, 28, 32-42. (IF = 1.9)
543. âSeparation, Characterisation and Biological Evaluation of the Individual Isomers of the Rat Selective Toxicant Norbormide â Isolated using a Chemical Derivatization Strategy,â M. Jay-Smith, Z. L. Wang, R. Al-Kassas, E. C. Murphy, Lee Shapiro, C. T. Eason, M. A. Brimble and D.Rennison, ARKIVOC, 2021, part x, 40-53. (IF = 1.0)
542. âInvestigating the Individual Importance of the Pam2Cys Ester Motifs on TLR2 Activity,â B. L. Lu, F. F. Li, I. D. Kelch, P. R. Dunbar, G. M. Williams and M. A. Brimble, European Journal of Organic Chemistry, 2021, 39, 5415-5423. (IF = 2.8)
541. âVesiculin Derived from IGF-II Drives Increased Islet Cell Mass in a Mouse Model of Pre-diabetes,â K. L. Lee, G.M. Williams and M. A. Brimble, Islets, 2021, in press. (IF = 2.6)
540. âA Highly Efficient N-Mesityl Thiazolylidene for the Aliphatic Stetter Reaction: Stereoelectronic Quantification for Comparison of N Heterocyclic Carbene Organocatalysts,â E. S. Pearl, D. M. J. Fellner, T. SĂśhnel, D. P. Furkert and M. A. Brimble, Asian Journal of Organic Chemistry, 2021, 10, 2869-2875. (IF = 3.3) (VIP paper; Invited Article for 10th Anniversary Special Collection)
539. âSynthesis of the C4-C16 Polyketide Fragment of Portimines A and B,â X. Ding, H.R.M. Aitken, E.S. Pearl, D.P. Furkert and M. A. Brimble, Journal of Organic Chemistry, 2021, 86, 12840â12850. (IF = 4.4)
538. âCharacterisation of Agonist Signalling Profiles and Agonist-dependent Antagonism at PACAP-responsive Receptors: Implications for Drug Discovery,â Z. Tasma, A. Siow, P.W.R. Harris, M.A. Brimble, D.L. Hay and C. J. Walker, British Journal of Pharmacology, 2022, 179, 435-453. (IF = 8.7) (Invited Article Themed Issue: Advances in Migraine and Headache Therapy (BJP 75th Anniversary)
537. âScalable Biomimetic Syntheses of Paeciloketal B, 1-epi-Paeciloketal B and Bysspectin A,â E. K. Davison, C. E. Shepperson, Z. E. Wilson and M. A. Brimble, Journal of Natural Products, 2021, 84, 2345-2351. (IF = 4.05)
536. âThe Total Chemical Synthesis and Biological Evaluation of the Cationic Antimicrobial Peptides, Laterocidine and Brevicidine,â Y. Hermant, D. Palpal-latoc, N. Kovalenko, A. J. Cameron, M. A. Brimble and P.W.R. Harris, Journal of Natural Products, 2021, 84, 2165â2174. (IF = 4.05)
535. âAntibody responses to Collagen Peptides and Streptococcal Collagen like Proteins in Acute Rheumatic Fever Patients,â D. Pilapitiya, P. W. R. Harris, P. Hanson-Manful, R. McGregor, R. Kowalczyk, J. Raynes, L. Carlton, R. Dobson, M. Baker, M. A. Brimble, S. Lukomski, and N. Moreland, Pathogens and Disease, 2021, 79(6), https://doi.org/10.1093/femspd/ftab033. (IF = 2.2)
534. âDisruption of Metallostasis in the Anaerobic Human Pathogen Fusobacterium nucleatum by the Zinc Ionophore PBT2,â E. Van Zuylen, S. Ferguson, A. Hughes, D. K. Rennison, M. A. Brimble and G. Cook, ACS Infectious Diseases, 2021, 7, 2285â2298. (IF = 4.4)
533. âA Concise Synthetic Strategy Towards the Novel Calcium-Dependent Lipopeptide Antibiotic, Malacidin A and Analogues,â N. Kovalenko, G. K. Howard, J. Swain, Y. Hermant, A. J. Cameron, G. M. Cook, S. A. Ferguson, L. A. Stubbing, P.W.R. Harris and M. A. Brimble, Frontiers in Chemistry (Chemical Biology), 2021, 9, article 687875, doi: 10.3389/fchem.2021.687875. (Invited Article for Special Issue âSecondary Metabolites and Peptides as Unique Natural Reservoirs for New Therapeutic Leads for Treatment of Cancer and Microbial Infectionsâ hosted by M. L. Mangoni, B. Botta and F. Ghirga). (IF = 3.99)
532. âPharmacological Characterisation of Mouse Calcitonin and Calcitonin Receptor-like Receptors Reveals Differences Compared to Human Receptors,â M. L. Garelja, R. L. Bower, M. A. Brimble, S. Chand, P.W.R. Harris, M. A. Jamaluddin, J. Petersen, A. Siow, C.S. Walker and D. L. Hay, British Journal of Pharmacology, 2022, 179, 416-434. (IF = 8.7) (Invited Article Themed Issue: Advances in Migraine and Headache Therapy (BJP 75th Anniversary)
531. âFourth Generation Analogues of the Anticancer Peptaibol Culicinin D: Probing the Effects of Hydrophobicity and Halogenation on Cytotoxicity,â J. K. Kasim, I. Kavianinia, M. Bull, P. W. R. Harris, J. B. Smaill, A. V. Patterson and M. A. Brimble, Synthesis, 2021, 4239-4245. (IF = 3.1) (IF = 3.1) (Special Issue in honour of Prof Sarah Reisman as the recipient of the ACS Dr Margaret Faul Award Women in Chemistry Award)
530. âEngineering a Stable Complex of ERp44 with a Designed Peptide Ligand for Analyzing the Mode of Interaction of ERp44 with its Clients,â L. Hampe, P. W. R. Harris, B. Rushton, M. Radjainia, M.A. Brimble and Alok K. Mitra, Peptide Science (The American Peptide Society Journal), 2021, e24230, https://doi.org/10.1002/pep2.24230
529. âSynthesis and Characterization of Mono S-Lipidated Peptide Hydrogels: A Platform for the Preparation of Reactive Oxygen Species Responsive Materials,â â A. Rani, L. M. De Leon-Rodriguez, I. Kavianinia, D. J. McGilvray, D. E. Williams and M. A. Brimble, Organic and Biomolecular Chemistry, 2021, 19, 3665â3677. (IF = 3.6)
528. âAmylin Analog Pramlintide Induces Migraine-like Attacks in Patients,â H. Ghanizada, M. Al-Karagholi, Mohammad, C. Walker, N. Arngrim, T. Rees, J. Petersen, A. Siow, M. Mørch-Rasmussen, S. Tan, S. O’Carroll, P. Harris, L. Skovgaard, N. Joergensen, M. A. Brimble, J. Waite, B. Rea, L. Sowers, A. Russo, D. Hay and M. Ashina, Annals of Neurology, 2021, 89, 1157-1171. (IF = 9.0)
527. âScreening a Natural Product-inspired Library for Anti-Phytophthora Activities,â S. A. Lawrence, H. F. Robinson, D. P. Furkert, M. A. Brimble and M. L. Gerth, Molecules, 2021, 26, 1819-1828. https://doi.org/10.3390/molecules26071819 (IF = 4.4)
526. âAnalysis of Advanced Glycation End Products in Ribose-, Glucose- and Lactose-Crosslinked Gelatin to Correlate the Physical Changes Induced by Maillard Reaction in Films,â A. E. Etxeberria, P. A. Kilmartin, J. I. MatĂŠ; S. Prabakar, M. A. Brimble and R. Naffa, Food Hydrocolloids, 2021, 117, 106736-106750. (IF = 7.0)
525. âThiol-ene Enabled Preparation of S-Lipidated anti-HBV Peptides,â O. A. Shepperson, A. J. Cameron, C. J. Wang, P. W. R. Harris, J. A. Taylor and M. A. Brimble, Organic and Biomolecular Chemistry, 2020, 18, in press. (IF = 3.6) https://doi.org/10.1039/D0OB01997F
524. âTotal Synthesis of (Âą)-Leonuketal,â P. S. Grant, D. P. Furkert and M. A. Brimble, Organic Letters, 2020, 22, in press. (IF = 6.6) https://doi.org/10.1021/acs.orglett.0c03364
⢠(Selected for incusion in âSynthesis Workshopâ https://synthesis-workshop.com/, a website that has short videio episodes on total syntheses, named reactions and other topics.)
523. âTotal Synthesis of Allene-Containing Cyclic Tetrapeptide Pseudoxylallemycin C,â A. J. Cameron, C. Park, G. K. Howard, P.W. R. Harris and M. A. Brimble, Synlett, 2020, in press. (IF = 2.4) https://doi.org/10.1055/a-1282-6870
522. âC-2 Derivatized 8-Sulfonamidoquinolines as Antibacterial Compounds,â E. K. Davison, J. E. McGowan, F. F. Li, A. D. Harper, J. Y. Jeong, S. Mros, N. Harbison-Price, E. M. Van Zuylen, M. K. Knottenbelt, A. Heikal, S. A. Ferguson, M. A. McConnell, G. M. Cook, W. Krittaphol, G. F. Walker, M. A. Brimble and D. Rennison, Bioorganic and Medicinal Chemistry, 2020, in press. (IF = 3.1) https://doi.org/10.1016/j.bmc.2020.115837
521. âRapid and Simultaneous Analysis of Advanced Glycation End Products on Silica Hydride Column: Comparison of UV, Fluorescence, and Mass Spectrometry Detectors,â R. Naffa, J. Gaar, M. Durrani, W. Zhang, C. Maidment, I. Shehadi, G.Holmes, I. Kavianinia and M. A. Brimble, Separation Science Plus, 2020, in press. https://doi.org/10.1002/sscp.202000077
⢠(Front Cover Image).
520. âA Ring Closing Metathesis Approach to the Formal Synthesis of (+)-Callyspongiolide,â K.-Y. Ko, Z. E. Wilson, D. P. Furkert and M. A. Brimble, ChemCatChem, 2020, (IF = 4.9) https://doi.org/10.1002/cctc.202001139
⢠(Invited Article for Special Collection on The Catalysis of Ring Synthesis)
519. âOn-Resin Preparation of Allenamidyl Peptides: a Versatile Chemoselective Conjugation and Intramolecular Cyclisation Tool,â A. Cameron, P.W.R. Harris and M. A. Brimble, Angewandte Chemie International Edition, 2020, 59, 18054-18061. (IF = 12.1) https://doi.org/10.1002/anie.202004656
⢠(VIP paper â top 10% accepted manuscripts; Hot Article, Front Cover Image).
518. âNanoribbon Self-assembly and Hydrogel Formation from an N-Octanoyl Octapeptide Derived from the Antiparallel beta-Interface of a Protein Homotetramer, â A. Rani, I. Kavianinia, L. M. De Leon-Rodriguez, D. J. McGillivray, D. E. Williams and M. A. Brimble, Acta Biomaterialia, 2020, 114, 233-243. (IF = 7.2) https://doi.org/10.1016/j.actbio.2020.07.023
517. âAsymmetric Total Synthesis of the Naturally Occurring Antibiotic Anthracimycin,â E. K. Davison, J. L. Freeman, W. Zhang, W. M. Wuest, D. P. Furkert and M. A. Brimble, Organic Letters, 2020, 22, 5550-5554. (IF = 6.6) https://doi.org/10.1021/acs.orglett.0c01913
516. âDirected Self-Assembly of Peptide-Diketopyrrolopyrrole Conjugates â a Platform for Bio-Organic Thin Film Preparation,â A. Rani, I. Kavianinia, P. Hume, L. M. De Leon-Rodriguez, S. Kihara, D. E. Williams, D. J. McGillivray, Natalie O. V. Plank, Juliet Gerrard, Justin M. Hodgkiss and M. A. Brimble, Soft Matter, 2020, 6563-6571. (IF = 3.4) https://doi.org/10.1039/D0SM01071E
⢠(Invited Article for Special Issue: Peptide Soft Materials)
515. âSynthesis and Biological Evaluation of S-Lipidated Lipopeptides of a Connexin 43 Channel Inhibitory Peptide,â S.-H. Yang, C. Clemett, M. A. Brimble, S. OâCarroll and P. W. R. Harris, RSC Medicinal Chemistry, 2020, 11, 1041â1047. (pending impact factor) https://doi.org/10.1039/D0MD00172D
514. âSynthesis and Antiproliferative Activity of C- and N-Terminal Analogues of Culicinin D,â F. F. Li, L. A. Stubbing, Kavianinia, M. R. Abbattista, P. W. R. Harris, J. B. Smaill, A. V. Patterson and M. A. Brimble, Bioorganic and Medicinal Chemistry Letters, 2020, 30, 127331-127337. (IF = 2.4) https://doi.org/10.1016/j.bmcl.2020.127331
513. âThiol-ene Enabled Chemical Synthesis of Truncated S-Lipidated Teixobactin Analogues,â V. V. Yim, A. J. Cameron, I. Kavianinia, P. W. R. Harris and M. A. Brimble, Frontiers in Chemistry (Chemical Biology), 2020, (IF = 3.8) https://doi.org/10.3389/fchem.2020.00568
⢠(Invited Article Special Issue: Women in Science: Chemistry)
512. âCLipPâing on Lipids to Generate Antibacterial Lipopeptides,â V. Yim, I. Kavianinia, M. K. Knottenbelt, S. A. Ferguson, G. M. Cook, S. Swift, A. Chakraborty, J. R. Allison, A. J. Cameron, P. W. R. Harris and M. A. Brimble, Chemical Science, 2020, 11, 5759-5765. (IF = 9.1) https://doi.org/10.1039/D0SC01814G
511. âSynthesis of Paenipeptin CĘš Analogues Employing Solution-Phase CLipPA Chemistry,â J. T. W. Tong, I. Kavianinia, S. A. Fergusson, G. M. Cook, P. W. R. Harris and M. A. Brimble, Organic and Biomolecular Chemistry, 2020, 18, 4381-4385. (IF = 3.6) https://doi.org/10.1039/D0OB00950D
510. âDesign, Characterization and Evaluation of ď˘-Hairpin Peptide Hydrogels as Support for Osteoblast Cell Growth and Bovine Lactoferrin Delivery,â L. M. De Leon-Rodriguez, Y.-E. Park, D. Naot, D. S. Musson, J. Cornish and M. A. Brimble, RSC Advances, 2020, 10, 18222-18230. (IF = 3.05) https://doi.org/10.1039/D0RA03011B
509. âGuanidinylated Amphiphilic Polycarbonates with Enhanced Antimicrobial Activity by Extending the Length of the Spacer Arm and Micelle Self-Assembly,â C. A. H. Cho, C. Liang, J. Perera, M. A. Brimble, S. Swift, and J. Jin, Macromolecular Bioscience, 2020, (IF = 2.9) https://doi.org/10.1002/MABI.202000065.
⢠(Front Cover Image)
508. âVariable-length Ester-based Staples for Îą-Helical Peptides Using A Double Thiol-ene Reaction,â D. L. Paterson, J. U. Flanagan, P. R. Shepherd, P. W. R. Harris and M. A. Brimble, Chemistry: A European Journal, 2020, 26, 10826-10833. (IF = 5.2) https://doi.org/10.1002/chem.202001478
507. âUtility of the Leptospermum Scoparium Compound Lepteridine as a Chemical Marker for Manuka Honey Authenticity,â B. Lin, B. J. Daniels, M. J. Middleditch, D. P. Furkert, M. A. Brimble, J. Bonga, J. M. Stephens and K. M. Loomes, ACS Omega, 2020, 5, 8858-8866. (IF = 2.6) https://doi.org/10.1021/acsomega.0c00486
506. âAlanine Scan-guided Synthesis and Biological Evaluation of Analogues of Culicinin D, a Potent Anticancer Peptaibol,â I. Kavianinia, L. A. Stubbing, M. R. Abbattista, P. W. R. Harris, J. B. Smaill, A. V. Patterson and M. A. Brimble, Bioorganic and Medicinal Chemistry Letters, 2020, 30, 127135. (IF = 2.4) https://doi.org/10.1016/j.bmcl.2020.127135
505. âSynthesis of Isotopically Labelled ÎąCGRP8-37 and its Lipidated Analogue,â B. L. Lu, K. M. Loomes, D. L. Hay, P. W. R. Harris and M. A. Brimble, Journal of Labelled Compounds and Radiopharmaceuticals, 2020, 1-8. (IF = 1.3) https://doi.org/10.1002/jlcr.3838
504. âResults of a Randomized, Double-Blind Phase II Clinical Trial of NY-ESO-1 Vaccine with ISCOMATRIXÂŽ Adjuvant Versus ISCOMATRIXÂŽ Alone in Participants with High Risk Resected Melanoma,â Journal for ImmunoTherapy of Cancer, J. S. Cebon, M. Gore, J. F. Thompson, I. D. Davis, G. A. McArthur, E. Walpole, M. Smithers, V. Cerundolo, P. R. Dunbar, D. MacGregor, C. Fisher, M. Millward, P. Nathan, M. P. N. Findlay, Peter Hersey, T. R. J. Evans, C. H. Ottensmeier, J. Marsden, A. G. Dalgleish, P. G. Corrie, M. Marples, M. A. Brimble, G. M. Williams, S. Winkler, L. Endo-Munoz1, C. S. A. Tutuka, R. Venhaus, L. J. Old, D. Haack, E. Maraskovsky, A. Behren and W. Chen, Journal for ImmunoTherapy of Cancer, 2020, 8, e000410. (IF = 8.7) https://doi.org/10.1136/jitc-2019-000410
503. âMultiple Bactericidal Mechanisms of the Zinc Ionophore PBT2,â N. Harbison-Price, S. Ferguson, A. Heikal, G. Taiaroa, K. Hards, Y. Nakatani, D. Rennison, M. A. Brimble, I. El Deeb, L. Bohlmann, C. McDevitt, M. von Itzstein, M. Walker and G. Cook, mSphere (American Society for Microbiology), 2020, 5:e00157-20; (IF = 4.4) https:// doi.org/10.1128/mSphere.00157-20
502. âSynthesis of Peptide Homo- and Heterodimers as Potential Mimics of PDGF-BB,â L. A. Stubbing, H. Kaur, S. X. Feng, M. Aalderink, M. Dragunow and M. A. Brimble, Peptide Science (The American Peptide Society Journal), 2020, 112, e24150. (IF = 2.0) https:// doi.org/10.1002/pep2.24150
⢠(Invited Article Special Issue honoring the lifetime achievements of Louis Carpino)
501. âDirect Synthesis of Cyclic Lipopeptides using Intramolecular Native Chemical Ligation and Thiol-ene CLipPA Chemistry,â V. V. Yim, I. Kavianinia, A. J. Cameron, P. W. R. Harris and M. A. Brimble, Organic and Biomolecular Chemistry, 2020, 18, 2838-2844. (IF = 3.6) https://doi.org/10.1039/D0OB00203H
⢠(Front Cover image and HOT article https://pubs.rsc.org/en/journals/articlecollectionlanding?sercode=ob&themeid=8400b4e4-d6c4-4fb9-a31f-b236dae3e39f)
500. âIntermolecular Diels-Alder Cycloaddition/Cross-coupling Sequences of 2-Bromo-1,3-Butadienes,â H. Choi, H. Shirley, H. Aitken, T. Schulte, T. SĂśhnel, P. Hume, M. A. Brimble and D. P. Furkert, Organic Letters, 2020, 22, 1022-1027. (IF = 6.6) https://doi.org/10.1021/acs.orglett.9b04567
⢠(Used for video for undergraduate organic chemistry students @chemhelpASAP; bit.ly/Brimble_vid)
499. âReplacement of the Acrid tert-Butylthiol and an Improved Isolation Protocol for Cysteine Lipidation on a Peptide or Amino Acid (CLipPA),â S.-H. Yang, Y. O. J. Hermant, P. W. R. Harris and M. A. Brimble, European Journal of Organic Chemistry, 2020, 36, 944-947. (IF = 3.1) https://doi.org/10.1002/ejoc.201901696
498. âSubstituted Sulfonamide Bioisosteres of 8-Hydroxyquinoline as Zinc-dependent Antibacterial Compounds,â Bioorganic and Medicinal Chemistry, D. Rennison, J. E McGowan, A. D. Harper, E. K. Davison, J. Y. Jeong, S. Mros, N. Harbison-Price, E. M. Van Zuylen, M. K. Knottenbelt, A. Heikal, S. A. Ferguson, M. A. McConnell, G. M. Cook, W. Krittaphol, G. F. Walker and M. A. Brimble, Bioorganic and Medicinal Chemistry, 2020, 28, 127110. (IF = 3.1) https://doi.org/10.1016/j.bmcl.2020.127110
497. âA Catalytic Asymmetric Ene Reaction For Direct Preparation of ďĄ-Hydroxy-1,4-Diketones As Intermediates In Natural Product Synthesis,â H. R. M. Aitken, D. P. Furkert and M. A. Brimble, Synlett, 2020, 31, 687-690. (IF = 2.4) https://doi.org/10.1055/s-0037-1610748
496. âAdvanced Glycated Apo A-IV Loses its Ability to Prevent the LPS-induced Reduction in Cholesterol Efflux-related Gene Expression in Macrophages,â L. Okuda, R. T. Iborra, P. R. Pinto, U. F. Machado, M. L. C. Correa-Giannella, R. Pickford, T. Woods, M. A. Brimble, K.-A. Rye and M. Passarelli, Mediators of Inflammation, 2020, vol 2020, p. 1-11. (IF = 3.5) https://doi.org/10.1155/2020/6515401
495. âDistinct Patterns of Internalization of Different Calcitonin Gene-related Peptide Receptors,â J. Gingell, T. Rees, E. Hendrikse, A. Siow, D. Rennison, J. Scotter, P. Harris, M. A. Brimble, C. Walker and D. Hay, ACS Pharmacology and Translational Science, 2020, 3, 296-304. https://doi.org/10.1021/acsptsci.9b00089
494. âMolecular Mechanisms of Class B GPCR Activation: Insights from Adrenomedullin Receptors,â M. Garelja, M. Au, M. A. Brimble, J. Gingell, E. Hendrikse, A. Lovell, N. Prodan, P. M. Sexton, A. Siow, C. Walker, H. Watkins, G. Williams, D. Wootten, S. Yang, P. Harris and D. Hay, ACS Pharmacology and Translational Science, 2020, 3, 246-262. https://doi.org/10.1021/acsptsci.9b00083
493. âSynthesis and SAR Analysis of Lipovelutibols B and D and their Lipid Analogues,â A. J. Cameron, E. K. Davison, C. An, L. A. Stubbing, P. R. Dunbar, P. W. R. Harris and M. A. Brimble, Journal of Organic Chemistry, 2020, 85, 1401-1406. (IF = 4.8) https://doi.org/10.1021/acs.joc.9b02348
⢠(Invited Article Special Issue âModern Peptide and Protein Chemistryâ)
492. âDivalent Cannabinoid-1 Receptor Ligands: A Linker Attachment Point Survey of SR141716A for Development of High-Affinity CB1R Molecular Probes,â P. S. Grant, N. Kahlcke, K. Govindpani, M. Hunter, C. MacDonald, M. A. Brimble, M. Glass and D. P. Furkert, Bioorganic and Medicinal Chemistry Letters, 2019, 29, 126644-126651. (IF = 2.42) https://doi.org/10.1016/j.bmcl.2019.126644
491. âA Versatile Boc Solid Phase Synthesis of Daptomycin and Analogues using Site Specific, On-resin Ozonolysis to Install the Kynurenine Residue,â B. Xu, Y. Hermant, S.-H. Yang, P. W. R. Harris and M. A. Brimble, Chemistry: A European Journal, 2019, 25, 14101-14107. (IF = 5.2) https://doi.org/10.1002/chem.201903725
⢠(Inside Front Cover image)
490. âSynthesis and Evaluation of Novel TLR2 Agonists as Potential Adjuvants for Cancer Vaccines,â B. Lu, G. M. Williams, D. Verdon, P. R. Dunbar and M. A. Brimble, Journal of Medicinal Chemistry, 2020, 63, 2282-2291. (IF = 6.3) https://doi.org/10.1021/acs.jmedchem.9b01044
⢠(Invited Article for the Special Issue âWomen in Medicinal Chemistryâ)
489. âSynthesis of the Tetracyclic Cores of the Integrastatins, Epicoccolide A and Epicocconigrone A,â J. Jeong, J. Sperry and M. A. Brimble, Journal of Organic Chemistry, 2019, 84, 11935-11944. (IF = 4.8) https://doi.org/10.1021/acs.joc.9b01796
488. âMicrotiter Screening Reveals Oxygen-Dependent Antimicrobial Activity of Natural Products Against Mastitis-Causing Bacteria,â S. A. Ferguson, A. Menorca, E. M. Van Zuylen, C.-Y. Cheung, M. McConnell, D. Rennison, M. A. Brimble, K. Bodle, S. McDougall, G. M. Cook and A. Heikal, Frontiers in Microbiology: Antimicrobials, Resistance and Chemotherapy, 2019, 10, 1995. https://doi.org/10.3389/fmicb.2019.01995
487. âPharmacological Characterization and Investigation of N-Terminal Loop Amino Acids of Adrenomedullin 2 that are Important for Receptor Activation,â H. Musa, E. R. Hendrikse, M. A. Brimble, M. L. Garelja, H. A. Watkins, P. W. R. Harris, D. L. Hay, Biochemistry, 2019, 58, 3468-3474. (IF = 3.0) https://doi.org/10.1021/acs.biochem.9b00571
486. âA Chiral Auxiliary-Based Synthesis of the C5-C17 trans-Decalin Framework of Anthracimycin,â J. Freeman, D. P. Furkert and M. A. Brimble, Organic Chemistry Frontiers, 2019, 6, 2954-2963. (IF = 5.5) https://doi.org/10.1039/C9QO00769E
485. âHighly Diastereoselective Synthesis of syn-1,3-Dihydroxyketone Motifs from Propargylic Alcohols via Unusual Spiroepoxide Intermediates,â X.Ding, D. P. Furkert and M. A. Brimble, Angewandte Chemie International Edition, 2019, 58, 11830-11835. (IF = 12.1) https://doi.org/10.1002/anie.201905736
484. âSynthesis and Antiproliferative Activity of Culicinin D Analogues Containing Simplified AHMOD-based Residues,â L. A. Stubbing, I. Kavianinia, M. R. Abbattista, P. W. R. Harris, J. B. Smaill, A. V. Patterson and M. A. Brimble, European Journal of Medicinal Chemistry, 2019, 177, 235-246. (IF = 5.1) https://doi.org/10.1016/j.ejmech.2019.05.052
483. âThe Selective Rat Toxicant Norbormide Blocks KATP Channels in Smooth Muscle Cells but not in Insulin-Secreting Cells,â F. Fusi, S. Bova, S. Saponara, A. Trezza, O. Spiga, B. Hopkins, D. Rennison and M. A Brimble, Frontiers in Pharmacology (Cardiovascular and Smooth Muscle Pharmacology section), 2019, 10, 598. (IF = 4.4) https://doi.org/10.3389/fphar.2019.00598
482. âGlucoregulatory Activity of Vesiculin in Insulin Sensitive and Resistant Mice,â K. L. Lee, J. F. Aitken, G. M. Williams, M. A. Brimble and G. J. S. Cooper, Peptides, 2019, 116, 1-7. (IF = 2.85) https://doi.org/10.1016/j.peptides.2019.04.011
481. âSite-specific Glycations of Aβ1â42 Affect Fibril Formation and are Neurotoxic,â J. Ng, H. Kaur, T. Collier, K. Chang, A. E. S. Brooks, J. R. Allison, M. A. Brimble, A. Hickey and N. P. Birch, J. Biol. Chem., 2019, 294, 8806-8818. (IF = 4.0) https://doi.org/10.1074/jbc.ra118.006846
480. âA Potent Fluorescent CGRP Analogue Enables Visualisation of Receptor Internalisation,â L. R. Yule, M. L. Garelja, E. H. Hendrikse, J. G. Gingell, D. R. Poyner, P. W. R. Harris, M. A. Brimble, D. L. Hay, Peptide Science, 2019, 111:e24126. (IF = 2.0) https://doi.org/10.1002/pep2.24126
479. âLive Applications of Norbormide-based Fluorescent Probes in Drosophila melanogaster,â A. Forgiarini, Z. Wang, C, D’Amore, M. Jay-Smith, F. F. Li, B. Hopkins, M. A. Brimble, A, Pagetta, S. Bersani, S. De Martin, B. Napoli, S. Bova, D. Rennison, G. Orso, PLOS ONE, 2019, 14: e0211169. (IF = 2.8) https://doi.org/10.1371/journal.pone.0211169
478. âInvestigations of the Key Macrolactamisation Step in the Synthesis of Cyclic Antimicrobial Tetrapeptide Pseudoxylallemycin A,â A. J. Cameron, C. J. Squire, A. GĂŠrenton, L. A. Stubbing, P. W. R. Harris and M. A. Brimble, Organic and Biomolecular Chemistry, 2019, 17, 3902-3913. (IF = 3.6) https://doi.org/10.1039/C9OB00227H
⢠(Highlighted by H. Yamamoto and A. Banerjee, Synfacts, 2019, 15, 825)
477. âSynthesis of Endolides A and B; Naturally Occurring N-Methylated Cyclic Tetrapeptides,â E. K. Davison, A. J. Cameron, P. W. R. Harris and M. A. Brimble, MedChemComm, 2019, 10, 693-698. (IF = 3.6) https://doi.org/10.1039/C9MD00050J
⢠(Invited Article for Special Issue on Natural Products, Selected for Front Cover image)
476. âConvenient Access to 5-Membered Cyclic Iminium Ions: Evidence for a Stepwise [4+2] Cycloaddition Mechanism,â J. L. Freeman, D. P. Furkert and M. A. Brimble, Organic and Biomolecular Chemistry, 2019, 17, 2705-2714. (IF = 3.6) https://doi.org/10.1039/C9OB00262F
475. âEnhancing T Cell Responses and Tumour Immunity by Vaccination with Peptides Conjugated to a Weak NKT Cell Agonist,â B. J. Compton, K. J. Farrand, C.-W. Tang, T. L. Osmond, M. Speir, A. Authier-Hall, J. Wang, P. M. Ferguson, S. T. S. Chan, R. J. Anderson, T. R. Cooney, C. M. Hayman, G. M. Williams, M. A. Brimble, C. R. Brooks, L.-K. Yong, L. S. Metelitsah, D. M. Zajonc, D. I. Godfrey, O. Gasser, R. Weinkove, G. F. Painter and I. F. Hermans, Organic and Biomolecular Chemistry, 2019, 17, 1225-1237. (IF = 3.6) https://doi.org/10.1039/C8OB02982B
474. âStructure-Activity Relationships of Wollamide Cyclic Hexapeptides with Activity against Drug-resistant and Intracellular Mycobacterium tuberculosis,â Z. Khalil, T. Hill, L. De Leon Rodriguez, R.-J. Lohman, H. Hoang, N. Reiling, D. Hillemann, M. A. Brimble, D. Fairlie, A. Blumenthal and R. Capon, Antimicrobial Agents and Chemotherapy, 2019, 63, e01773-18. (IF = 4.5) https://doi.org/10.1128/AAC.01773-18
473. âEfficient Synthesis and Characterisation of the Amyloid Beta Peptide, Aβ1-42, using a Double Linker System,â J. K. Kasim, I. Kavianinia, J. Ng, P. W. R. Harris, N. P. Birch and M. A. Brimble, Organic and Biomolecular Chemistry, 2019, 17, 30-34. (IF = 3.6) https://doi.org/10.1039/C8OB02929F
472. âA Synthetic Approach to âClickâ Neoglycoprotein Analogues of EPO Employing One-pot Native Chemical Ligation and CuAAC Chemistry,â D. J. Lee, A. J. Cameron, T. H. Wright, P. W. R. Harris and M. A. Brimble, Chemical Science, 2019, 10, 815-828. (IF = 9.1) https://doi.org/10.1039/C8SC03409E
⢠Highlighted in Chemistry World: https://www.chemistryworld.com/news/erythropoietin-benefits-from-controlled-sugar-coating/3009861.article
471. âA Chemometric Analysis of Compounds from Native New Zealand Medicinal Flora,â L. I. Pilkington, X. Yang, M.-W. Liu, Y. Hemar, M.A. Brimble and JĂłhannes Reynisson, Chemistry- An Asian Journal, 2019, 14, 1117-1127. (IF = 3.7) https://doi.org/10.1002/asia.201800803
470. âSynthesis of the Bicyclic Lactone Core of Leonuketal Enabled by a Telescoped Diels-Alder Reaction Sequence,â P. S. Grant, M. A. Brimble and D. P. Furkert, Chemistry – An Asian Journal, 2019, 14, 1128-1135. (IF = 3.7) https://doi.org/10.1002/asia.201800903
⢠(Invited Article – Special Issue dedicated to Chemistry in New Zealand)
469. âSynthesis and Biological Characterization of a New Norbormide Derived Bodipy Fl-Conjugated Fluorescent Probe for Cell Imagingâ C. D’Amore, G. Orso, A. Forgiarini, G. Ceolotto, D. Rennison, G. Ribaudo, M. Jay Smith, B. Hopkins, M. A. Brimble and S. Bova, Frontiers in Pharmacology (Experimental Pharmacology and Drug Discovery), 2018, 9 (1055), 1-13. (IF = 4.4) https://doi.org/10.3389/fphar.2018.01055
468. âReactivity of 2-Nitropyrrole Systems: Strategic Evolution of Synthetic Approaches to Nitropyrrole Natural Products,â X.-B. Ding, M. A. Brimble and D. P. Furkert, Journal of Organic Chemistry, 2018, 83, 12460-12470. (IF = 4.8) https://doi.org/10.1021/acs.joc.8b01692
467. âGenome Mining, Isolation, Chemical Synthesis and Biological Evaluation of a Novel Lanthipeptide, Tikitericin and N-Truncated Analogues, from the Extremophilic Microorganism Thermogemmatispora Strain T81,â B. Xu, E. J. Aitken, B. P. Baker, C. Turner, J. E. Harvey, M. B. Stott, J. F. Power, P. W.R. Harris, R. A. Keyzers and M. A. Brimble, Chemical Science, 2018, 9, 7311-7317. (IF = 9.1) https://doi.org/10.1039/C8SC02170H
⢠(Selected as Article for Chemical Science âPick of the Weekâ and for Back Cover)
466. âCardiac Troponins may be Irreversibly Modified by Glycation: Novel Potential Mechanisms of Cardiac Performance Modulation,â J. Janssens, B. Ma, M. A. Brimble, J. Van Eyk, L. Delbridge and K. Mellor, Scientific Reports â Nature, 2018, 8, 16084-16098. (IF = 4.1) https://doi.org/10.1038/s41598-018-33886-x
465. âSolid-Phase Thiol-ene Lipidation of Peptides for the Synthesis of a Potent CGRP Receptor Antagonist,â E. T. Williams, P. W. R. Harris, M. A. Jamaluddin, K. M. Loomes, D. L. Hay and M. A. Brimble, Angewandte Chemie International Edition, 2018, 57, 11640-11643. (IF = 12.1) https://doi.org/10.1002/anie.201805208
464. âPhotoaffinity Cross-linking and Unnatural Amino Acid Mutagenesis Reveal Insights into Calcitonin Gene-related Peptide Binding to the Calcitonin Receptor-like Receptor/Receptor Activity-Modifying Protein 1 (CLR/RAMP1) Complex,â J. Simms, R. Uddin, T. Sakmar, J. Gingell, M. Garelja, D. Hay, M. A. Brimble, P. Harris, C. Reynolds, D. Poyner, ACS Biochemistry, 2018, 57, 4915-4922. (IF = 2.9) https://doi.org/10.1021/acs.biochem.8b00502
463. âTotal Synthesis of the Proposed Structure of Talarolide A,â S. Zhang, L. M. De Leon Rodriguez, R. Huang, I. K.H. Leung, P. W. R. Harris and M. A. Brimble, Organic and Biomolecular Chemistry, 2018, 16, 5286-5293. (IF = 3.6) https://doi.org/10.1039/C8OB01230J
462. âSupramolecular Threading of Peptide Hydrogel Fibrils,â N. Hauptstein, L. M. De Leon Rodriguez, A. K. Mitra, Y. Hemar, I. Kavianinia, N. Li, V. Castelletto, I. Hamley, M. A. Brimble, ACS Biomaterials Science and Engineering, 2018, 4, 2733-2738. (IF = 3.2) https://doi.org/10.1021/acsbiomaterials.8b00283
461. âSupplementation of Blackcurrant Anthocyanins increased Cyclic Glycine-Proline in the Cerebrospinal Fluid of Parkinson Patients, a Potential Treatment to improve Insulin-like Growth Factor-1 Function,â D. Fen, Y. Alamri, K. Liu, M. MacAskill, P. Harris, M. Brimble, J. Dalrymple-Alford, T. Anderson, T. Prickett, O.Menzies, A. Laurenson and J. Guan, Nutrients, 2018, 10, 714-725. (IF = 4.2) https://doi.org/10.3390/nu10060714
460. âTethering Fragment-Based Drug Discovery to Identify Inhibitors of the Essential Respiratory Membrane Protein Type II NADH Dehydrogenase,â A. Heikal, Y. Nakatani, W. Jia, C. Wilson, D. Rennison, M. R. Weimar, E. J. Parker and M. A. Brimble, G. M. Cook, Bioorganic and Medicinal Chemistry Letters, 2018, 28, 2239-2243. (IF = 2.4) https://doi.org/10.1016/j.bmcl.2018.05.048
459. âMolecular Signature for Receptor Engagement in the Metabolic Peptide Hormone Amylin,â R. Bower, L. Yule, T. Rees, G. Deganutti, E. Hendrikse, P. Harris, R. Kowalczyk, Z. Ridgway, A. Wong, K. Swierkula, D. Raleigh, A. Pioszak, M. A. Brimble, C. Reynolds, C. Walker and D. Hay, ACS Pharmacology and Translational Science, 2018, 1, 32-49. (new journal impact factor not available) https://doi.org/10.1021/acsptsci.8b00002
458. âThe Role for Cyclic Glycine-Proline, a Biological Regulator of Insulin-like Growth Factor-1 in Pregnancy-related Obesity and Weight Changes,â J. Guan, G. Singh-Mallah, K. Liu, E. Thorstensen, P. Shorten, E. A. Mitchell, R. Taylor, P. Harris, M. A. Brimble, J. M. D. Thompson and R. Murphy, Journal of Biological Regulators and Homeostatic Agents, 2018, 32, 11-25. (IF = 1.5) (no DOI, https://www.researchgate.net/publication/325905407_The_role_for_cyclic_Glycine-Proline_a_biological_regulator_of_insulin-like_growth_factor-1_in_pregnancy-related_obesity_and_weight_changes only link found with fill (proof) text available)
457. âDesacetyl-ďĄ-melanocyte Stimulating Hormone and ďĄ-Melanocyte Stimulating Hormone are required to Regulate Energy Balance,â K. G. Mountjoy, A. Caron, K. Hubbard, A. Shome, A. C. Grey, B. Sun, S. Bould, M. Middleditch, B. PontreĚ, A. McGregor, P. W. R. Harris, R. Kowalczyk and M. A. Brimble, R. Botha1, K. M. L. Tan, S. J. Piper, C. Buchanan, S. Lee, A. P. Coll and J. K. Elmquis, Molecular Metabolism, 2018, 9, 207-216. (IF = 6.8) https://doi.org/10.1016/j.molmet.2017.11.008
456. âTotal Synthesis of (-)-Peniphenone A,â M. Pantin, M. A. Brimble and D. P. Furkert, Journal of Organic Chemistry, 2018, 83, 7049-7059. (IF = 4.8) https://doi.org/10.1021/acs.joc.7b03231
⢠(Selected for Special Issue âSynthesis of Antibiotics and Related Moleculesâ)
455. âUsing Chemical Synthesis to Probe Structure-Activity Relationships of the Glycoactive Bacteriocin Glycocin F,â S. Bisset, S.-H. Yang, Z. Amso, P. Harris, M. Patchett, M. A. Brimble and G. Norris, ACS Chemical Biology, 2018, 13, 1270-1278. (IF = 5.0) https://doi.org/10.1021/acschembio.8b00055
454. âA Double-click Approach to the Protecting Group Free Synthesis of Glycoconjugates,â S. R. Alexander, G. M. Williams, M. A. Brimble and A. J. Fairbanks, Organic and Biomolecular Chemistry, 2018, 16, 1258-1262. (IF = 3.6) https://doi.org/10.1039/C8OB00072G
453. âReceptor Activity-Modifying Proteins have Limited Effects on the Class B G Protein-Coupled Receptor Calcitonin Receptor-like Receptor Stalk,â M. Garelja, C. Walker, A. Siow, S. Yang, P. Harris, M. A. Brimble, H. Watkins, J. Gingell and D. Hay, Biochemistry, 2018, 8, 1410-1422. (IF = 2.9) https://doi.org/10.1021/acs.biochem.7b01180
452. âTotal Synthesis and Conformational Study of The Anti-tubercular Cyclic Peptide Callyaerin A Bearing a Rare Rigidifying (Z)-2,3-Diaminoacrylamide Moiety,â M. A. Brimble, S. Zhang, L. M. De Leon Rodriguez, I. K. H. Leung, G. M. Cook and P. W. R. Harris Angewandte Chemie International Edition, 2018, 57, 3631-3635.
(IF = 12.1) https://doi.org/10.1002/ange.201712792
⢠(Selected for âCover Imageâ and as âVIP paperâ, < 10% of accepted papers receive this accolade; highlighted on ChemistryViews.org
see: http://www.chemistryviews.org/details/ezine/10879614/Total_Synthesis_of_Callyaerin_A.html)
451. âTotal Synthesis of the Highly N-Methylated Acetylene-Containing Anticancer Peptide Jahanyne,â A. Siow, G. Opiyo, I. Kavianinia, F. F. Li, D. P. Furkert, P. W. R Harris and M. A. Brimble, Organic Letters, 2018, 20, 788-791. (IF = 6.6) https://pubs.acs.org/doi/10.1021/acs.orglett.7b03925
450. âTotal Chemical Synthesis of Glycocin F and Analogues: S-Glycosylation Confers Improved Antimicrobial Activity,â Z. Amso, S. W. Bisset, S.-H. Yang, P. W. R. Harris, T. H. Wright, C. D. Navo, M. L. Patchett, G. E. Norris and M. A. Brimble, Chemical Science, 2018, 9, 1686-1691. (IF = 9.1) https://doi.org/10.1039/C7SC04383J
449. âMolecular Weight and Charge Density Effects of Guanidinylated Biodegradable Polycarbonates on Antimicrobial Activity and Selectivity,â C. A. H. Cho, C. Liang, J. Perera, J. Liu, K. G. Varnava, V. Sarojini, R. P. Cooney, D. J. McGillivray, M. A. Brimble, S. Swift and J. Jin, Biomacromolecules, 2018, 19, 1389-1401. (IF = 5.2) https://doi.org/10.1021/acs.biomac.7b01245
448. âAGE-Albumin Enhances ABCA1 Degradation by Ubiquitin-proteasome and Lysosomal Pathways in Macrophagesâ R. T. Iborra, A. Machado-Lima, L. S. Okuda, P. R. Pinto, E. R. Nakandakare, U. F. Machado, M. L. Correa-Giannella, R. Pickford, T. Woods, M. A. Brimble, K.-A. Rye, R. Lu, S. Yokoyama and M. Passarelli, Journal of Diabetes and its Complications, 2018, 32, 1-10. https://doi.org/10.1016/j.jdiacomp.2017.09.012
447. âA Phase I Vaccination Study with Dendritic Cells Loaded with NY-ESO-1 and alpha-Galactosylceramide: Induction of Polyfunctional T cells in High-risk Melanoma Patients,â O. Gasser, K. J. Sharples, C. Barrow, G. M. Williams, E. Bauer, C. E. Wood, B. Mester, M. Dzhelali, G. Caygill, J. Jones, C. M. Hayman, V. A. Hinder, J. Macapagal, M. McCusker, R. Weinkove, G. F. Painter, M. A. Brimble, M. P. Findlay, P. R. Dunbar and Ian F. Hermans, Cancer Immunology, Immunotherapy, 2018, 67, 285-298. (IF = 4.8) https://doi.org/10.1007/s00262-017-2085-9
446. âAnthranilate Phosphoribosyltransferase: Binding Determinants for 5â˛-Phospho-alpha-D-ribosyl-1â˛-pyrophosphate (PRPP) and the Implications for Inhibitor Designâ G. L. Evans, D. P. Furkert, N. Abermil, P. Kundu, K. M. de Lange, E. J. Parker, M. A. Brimble, E. N. Baker and J. S. Lott, Biochimica et Biophysica Acta (BBA) – Proteins and Proteomics, 2018, 1866, 264-274. (IF = 3.0) https://doi.org/10.1016/j.bbapap.2017.08.018
445. âAugmenting Influenza-Specific T Cell Memory Generation with a Natural Killer T Cell-Dependent Glycolipid-Peptide Vaccine,â R. J. Anderson, J. Li, L. Kedzierski, B. J. Compton, C. M. Hayman, T. L. Osmond, C.-W. Tang, K. J. Farrand, H.-F. Koay, C. F. D. S. S. E. Almeida, L. R. Holz, G. M. Williams, M. A. Brimble, Z. Wang, M. Koutsakos, K. Kedzierska, D. I. Godfrey, I. F. Hermans, S. J. Turner and G. F. Painter, ACS Chemical Biology, 2017, 12, 2898-2905. (IF = 5.0) https://doi.org/10.1021/acschembio.7b00845
444. âN-Acetylcysteine Counteracts Adipose Tissue Macrophage Infiltration and Insulin Resistance Elicited by Advanced Glycated Albumin in Healthy Rats,â K. S. Da Silva, P. R. Pinto, N. T. Fabre, D. J. Gomes, K. Thieme, L. S. Okuda, R. T. Iborra, V. G. Freitas, M. H. M. Shimizu, W. R. Teodoro, S. K. N. Marie, T. Woods, M. A Brimble, R. Pickford, K.-A. Rye, M. Okamoto, S. Catanozi, M. L. Correa-Giannela, U. F. Machado and M. Passarelli, Frontiers in Physiology, 2017, 8, 723. (IF = 4.0) https://dx.doi.org/10.3389%2Ffphys.2017.00723
443. âStereochemical Characterisation of Polyketide Stereotriads Synthesized via Hydrogen Mediated Asymmetric Syn-Crotylation,â M. Pantin, J. G. Hubert, T. SoĚhnel, M. A. Brimble and D. P. Furkert, Journal of Organic Chemistry, 2017, 82, 11225-11229 (IF = 4.8) https://doi.org/10.1021/acs.joc.7b01820
442. âSynthesis and Biological Evaluation of Novel Teixobactin Analogues,â C. E. Schumacher, P. W.R. Harris, X.-B. Ding, B. Krause, T. H. Wright, G. M. Cook, D. P. Furkert and M. A. Brimble, Organic and Biomolecular Chemistry, 2017, 15, 8755-8760. (IF = 3.6) https://doi.org/10.1039/C7OB02169K
441. âGeneral Synthesis of the Nitropyrrolin Family of Natural Products via Regioselective CO2-Mediated Alkyne Hydration,â X.-B. Ding, D. P. Furkert and M. A. Brimble, Organic Letters, 2017, 19, 5418-5421. (IF = 6.6) https://doi.org/10.1021/acs.orglett.7b02687
⢠(included in Organic Highlights: https://www.organic-chemistry.org/Highlights/2018/28May.shtm)
440. âUnderstanding the Metal Mediated Assembly and Hydrogel Formation of a β-Hairpin Peptide,â L. M. De Leon Rodriguez, Y. Hemar, A. K. Mitra and M. A. Brimble, Biomaterials Science, 2017, 5, 1993-1997. (IF = 4.2) https://doi.org/10.1039/C7BM00512A
439. âSynthesis and Incorporation of an Advanced Lipid Peroxidation End-product Building Block into Collagen Mimetic Peptides,â I. Kavianinia, S.âH. Yang, H. Kaur, P.W. R. Harris, R. C. J. Dobson, A. J. Fairbanks and M. A. Brimble, Chemical Communications, 2017, 53, 8459-8462. (IF = 6.5) https://doi.org/10.1039/c7cc05025a
438. âIncorporation of ‘Click’ Chemistry Glycomimetics Dramatically Alters Triple-helix Stability in an Adiponectin Model Peptide,â K. R. Lutteroth, P. W. R. Harris, T. H. Wright, H. Kaur, K. Sparrow, S.-H. Yang, G. J. S. Cooper and M. A. Brimble, Organic and Biomolecular Chemistry, 2017, 15, 5602-5608. (IF = 3.6) https://doi.org/10.1039/C7OB01388D
437. âBioinspired Total Synthesis and Stereochemical Revision of the Fungal Metabolite Pestalospirane B,â S. Badrinarayanan, C. J. Squire, J. Sperry and M. A. Brimble, Organic Letters, 2017, 19, 3414-3417. (IF = 6.6) https://doi.org/10.1021/acs.orglett.7b01371
⢠(selected for inclusion in ACS Select Collection focused on natural products total synthesis because of its high scientific quality and broad appeal).
436. âTotal Synthesis and Stereochemical Revision of the 2-Formylpyrrole Alkaloid Hemerocallisamine I,â J. M. Wood, D. P. Furkert and M. A. Brimble, Journal of Natural Products, 2017, 80, 1926-1929. (IF = 3.8) https://doi.org/10.1021/acs.jnatprod.7b00314
435. âNorborn-2-en-7-ones as Physiologically-Triggered Carbon Monoxide-Releasing Prodrugsâ J. T. B. Kueh, N. J. Stanley, R. J. Hewitt, L. M. Woods, L. Larsen, J. C. Harrison, D. Rennison, M. A. Brimble, I. A. Sammut, and D. S. Larsen, Chemical Science, 2017, 8, 5454-5459. (IF = 9.1) https://doi.org/10.1039/C7SC01647F
434. âStability of Polyelectrolyte-Coated Iron Nanoparticles for T2-Weighted Magnetic Resonance Imagingâ A. J. McGrath, C. Dolan, S. Cheong, D. A. J. Herman, B. Naysmith, F. Zong, P. Galvosas, K. J. Farrand, I. F. Hermans, M. A. Brimble, D. E. Williams, J. Jin, R. Tilley and R. D. Herman, Journal of Magnetism and Magnetic Materials, 2017, 439, 251-258. (IF = 2.4) https://doi.org/10.1016/j.jmmm.2017.04.026
433. âStructure-Activity Relationship Study of the Tumour-Targeting Peptide A20FMDV2 via Modification of Lys16, Leu13, and N- and/or C-Terminal Functionalityâ K.-Y. Hung, P. W. R. Harris, A. Desai, J. F. Marshall and M. A. Brimble, European Journal of Medicinal Chemistry, 2017, 136, 154-164. (IF = 3.5) https://doi.org/10.1016/j.ejmech.2017.05.008
432. âUnexpected Direct Synthesis of N-Vinyl Amides Through Vinyl Azide-Enolate [3+2] Cycloadditionâ H. Choi, H. J. Shirley, P. A. Hume, D. P. Furkert and M. A. Brimble, Angewandte Chemie International Edition, 2017, 56, 7420-7424. (IF = 12.0) https://doi.org/10.1002/anie.201702727
⢠(Selected by Editorial Board of Synfacts for its important insights; see: Synfacts 2017, 13(08), 0864; https://doi.org/10.1055/s-0036-1590632; Contributors: P.Knochel, J. M. Hammann
431. âRemarkable Influence of Cobalt Catalysis on Epoxide Ring-Opening with Sulfoxonium Ylidesâ M. L. Jamieson, N. Z. Brant, M. A. Brimble and D. P. Furkert, Synthesis, 2017, 49, 3952-3956. (IF = 2.7 ) : ) https://doi.org/10.1055/s-0036-1588814
⢠(Invited Feature Article and Special Topic âCobalt in Organic Synthesisâ Cover Page, Synthesis, 2017, 49, 3885; DOI: 10.1055/s-0036-1589510)
430. âProtecting Group Free Synthesis of Glycosyl Thiols from Reducing Sugars in Water; Application to the Production of N-glycan Glycoconjugatesâ S. R. Alexander, D. Lim, Z. Amso, M. A. Brimble and A. J. Fairbanks, Organic and Biomolecular Chemistry, 2017, 15, 2152-2156. (IF = 3.6) https://doi.org/10.1039/C7OB00112F
429. âMALDI-Imaging Enables Direct Observation of Kinetic and Thermodynamic Products of Mixed Peptide Fiber Assemblyâ K. Medini, B. West, D. E. Williams, M. A. Brimble and J. A. Gerrard, Chemical Communications, 2017, 53, 1715-1718. (IF = 6.4) https://doi.org/10.1039/C6CC10146A
428. âCyclization of Linear Tetrapeptides Containing N-Methylated Amino Acids by Using 1-Propanephosphonic Acid Anhydrideâ S. Zhang, L. M. De Leon Rodriguez, E. Lacey, A. M. Piggott, I. K. H. Leung and M. A. Brimble, European Journal of Organic Chemistry, 2017, 33, 149-158. (IF = 3.1) https://doi.org/10.1002/ejoc.201601016
427. âAn Efficient Chemical Synthesis of Lassomycin Enabled by an On-resin Lactamisation-Off-resin Methanolysis Strategy and Preparation of Chemical Variantsâ P. W. R. Harris, G. M. Cook, I. K. H. Leung and M. A. Brimble, Australian Journal of Chemistry, 2017, 70, 172-183. (IF = 1.226) http://dx.doi.org/10.1071/CH16499
⢠(Invited Article for Special Edition on âPeptide Chemistryâ and selected for inclusion in Special Virtual Issue devoted to the best of local medicinal chemistry in the past 5 years see: https://www.publish.csiro.au/ch/virtualissue/2942)
426. âCharacterizing the Mode of Action of Extracellular Connexin43 Channel Blocking Mimetic Peptides in an in vitro Ischemia Injury Modelâ Y. Kim, J. M. Griffin, P. W. R. Harris, S. H. C. Chan, L. F. B. Nicholson, M. A. Brimble, S. J O’Carroll and C. R. Green, Biochimica and Biophysica Acta (General), 2017, 1861, 68-78. (IF = 5.08) https://doi.org/10.1016/j.bbagen.2016.11.001
425. âMultifunctional Thermoresponsive Designer Peptide Hydrogelsâ L. M. De Leon Rodriguez, Y. Hemar, G. Mo, A. K. Mitra, J. Cornish and M. A. Brimble, Acta Biomaterialia, 2017, 47, 40-49. (IF = 6.1) https://doi.org/10.1016/j.actbio.2016.10.014
⢠(Highlighted in Gyros Protein Technologies Newsletter, https://cdn2.hubspot.net/hubfs/378579/1-PTI/emailers/Review%20Article/Multifunctional%20thermoresponsive%20peptide%20hydrogels%20designed%20to%20meet%20the%20demands%20of%20biomedical%20applications.pdf?hsCtaTracking=8e443296-781b-4086-b13f-1db4bcf1d20b%7C8653de01-2be4-4790-aa07-a17b1f3f9ba; 3000 subscribers)
424. âSolid-Phase Synthesis of the Peptaibol Alamethicin U-22324 Using a Double-Linker Strategyâ A. Siow, K.-Y. Hung, P. W. R. Harris and M. A. Brimble, European Journal of Organic Chemistry, 2017, 350-354. (IF = 3.1) https://doi.org/10.1002/ejoc.201601102
423. â2-Nitropyrrole Cross-Coupling Enables a Second Generation Synthesis of the Heronapyrrole Antibiotic Natural Product Familyâ X. Ding, D. P. Furkert and M. A. Brimble, Chemical Communications, 2016, 52, 12638-12641. (IF = 6.4) https://doi.org/10.1039/C6CC07532K
422. âA NBD Derivative of the Selective Rat Toxicant Norbormide as a New Probe for Living Cell Imagingâ
C. D’Amore, G. Orso, F. Fusi, M. A. Pagano, G. Miotto, A. Forgiarini, S. De Martin, G. Castellani, G. Ribaudo, D. Rennison, M. A. Brimble, B. Hopkins, A. Ferrarese and S. Bova, Frontiers in Pharmacology (Experimental Pharmacology and Drug Discovery), 2016, 7(315), 1-13. (IF = 4.4) Open Access Article. http://dx.doi.org/10.3389/fphar.2016.00315
421. âCyclic Enecarbamates as Precursors of alpha,beta-Unsaturated Iminium Ions: Reactivity and Synthesis of 6,6-Spirocyclic Ring Systemsâ Z. Wang, N. Krogsgaard-Larsen, B. Daniels, D. P. Furkert and M. A. Brimble, Journal of Organic Chemistry, 2016, 81, 10366-10375 (IF = 4.8) https://doi.org/10.1021/acs.joc.6b01343
420. âGlycated Albumin Induces Lipid Infiltration in Mice Aorta Independently of DM and RAS Local Modulation by Inducing Lipid Peroxidation and Inflammationâ D. J. Gomes, A. P. Velosa, L. S. Okuda, F. B. Fusco, K. S. da Silva, P. R. Pinto, E. R. Nakandakare, M. L. Correa-Giannella, T. Woods, M. A. Brimble, R. Pickford, K.-A. Rye, W. R. Teodoro, S. Catanozi and M. Passarelli, Journal of Diabetes and Its Complications, 2016, 30, 1614-1621. (IF = 2.0) https://doi.org/10.1016/j.jdiacomp.2016.07.001
419. âStructure Activity Relationship Study on the Peptide Hormone Preptin, a Novel Bone-anabolic Agent for the Treatment of Osteoporosisâ Z. Amso, R. Kowalczyk, M. Watson, Y.-E. Park, K. E. Callon, D. S. Musson, J. Cornish and M. A. Brimble, Organic and Biomolecular Chemistry, 2016, 14, 9163-9440 (IF = 3.6) https://doi.org/10.1039/C6OB01455K
⢠(Selected for âFront Coverâ)
418. âTotal Synthesis and Stereochemical Revision of the Anti-Tuberculosis Peptaibol Trichoderin Aâ I. Kavianinia, L. Kunalingam, P. W. R. Harris, G. M. Cook and M. A. Brimble, Organic Letters, 2016, 18, 3878-3881. (IF = 6.6) https://doi.org/10.1021/acs.orglett.6b01886
417. âTotal Synthesis of the Resorcyclic Acid Lactone Spiroketal Citreoviranolâ R. Quach, D. P. Furkert and M. A. Brimble, Journal of Organic Chemistry, 2016, 81, 8343-8350. (IF = 4.8) https://doi.org/10.1021/acs.joc.6b01503
416. âSynthesis of Psychrophilin Eâ S. T. Y. Ngen, H. Kaur, P. A. Hume, D. P. Furkert and M. A. Brimble, Journal of Organic Chemistry, 2016, 81, 7635-7643. (IF = 4.8) https://doi.org/10.1021/acs.joc.6b01369
415. âSynthesis of the 2-Formylpyrrole Spiroketal Pollenopyrroside A and Structural Elucidation of Xylapyrroside A, Shensongine A and Capparisine Bâ J. M. Wood, D. P. Furkert and M. A. Brimble, Organic and Biomolecular Chemistry, 2016, 14, 7569-7664. (IF = 3.6) https://doi.org/10.1039/C6OB01361A
414. âMaternally Administered Cyclic-Glycine-Proline Increases Insulin-like Growth Factor-1 Bioavailability and Novelty Recognition in Developing Offspringâ G. Singh-Mallah, K. Singh, C. D. McMahon, P. Harris, M. A. Brimble, E. Thorstensen and J. Guan, Endocrinology, 2016, 157, 3130-3139. (IF = 4.4) https://doi.org/10.1210/en.2016-1189
413. âSynthesis and Biological Evaluation of Analogues of the Potent ADAM8 Inhibitor Cyclo(RLsKDK) for the Treatment of Inflammatory Diseases and Cancer Metastasisâ V. Yim, A. F. M. Noisier, K.-Y. Hung, J. W. Bartsch, U. Schlomann and M. A. Brimble, Bioorganic and Medicinal Chemistry, 2016, 24, 4032-4037. (IF = 2.8) https://doi.org/10.1016/j.bmc.2016.06.042
412. âStereoselective Synthesis of the Rat Selective Toxicant Norbormideâ M. Jay-Smith, E. C. Murphy, L. Shapiro, C. T. Eason, M. A. Brimble and D. Rennison, Tetrahedron, 2016, 72, 5331-5342. (IF = 2.6) https://doi.org/10.1016/j.tet.2016.07.014
411. âSynthesis of Natural Cyclopentapeptides Isolated from Dianthus chinensisâ S. Zhang, Z. Amso, L. M. De Leon Rodriguez, H. Kaur and M. A. Brimble, Journal of Natural Products, 2016, 79, 1769â1774. (IF = 3.8) https://doi.org/10.1021/acs.jnatprod.6b00152
410. âIdentification of Anticancer Agents Based on the Thieno[2,3-b]pyridine and 1H-Pyrazole Molecular Scaffoldsâ C. Eurtivong, I. ReynisdĂłttir, S. Kuczma, D. P. Furkert, M. A. Brimble and J. Reynisson, Bioorganic and Medicinal Chemistry, 2016, 24, 3521-3526. (IF = 2.8) https://doi.org/10.1016/j.bmc.2016.05.061
409. âSynthesis and in vitro Bone Cell Activity of Analogues of the Cyclohexapeptide Dianthin Gâ Z. Amso, R. Kowalczyk, Y.-E. Park, M. Watson, J.-M. Lin, D. S. Musson, J. Cornish and M. A. Brimble, Organic and Biomolecular Chemistry, 2016, 14, 6231-6243. (IF = 3.6) https://doi.org/10.1039/c6ob00983b
⢠(Invited article for âSelective Chemistry with Peptides and Proteinsâ themed issue edited by Professor Phil Dawson)
408. âIsolation, Structural Elucidation and Synthesis of Lepteridine from MÄnuka (Lepstospermum scoparium) Honeyâ B. J. Daniels, G. Prijic, S. Meidinger, K. M. Loomes, J. M. Stephens, R. C. Schlothauer, D. P. Furkert and M. A. Brimble, Journal of Agricultural and Food Chemistry, 2016, 64, 5079â5084. (IF = 2.9) https://doi.org/10.1021/acs.jafc.6b01596
407. âControlling Gelation with Sequence: Towards Programmable Peptide Hydrogelsâ K. Medini, B. W. Mansel, M. A. K. Williams, M. A. Brimble, D. E. Williams, J. A. Gerrard, Acta Biomaterialia, 2016, 43, 30-37. (IF = 6.1) https://doi.org/10.1016/j.actbio.2016.07.021
406. âSubstituted Carbazoles â A New Class of Anthelmintic Agentâ D. Rennison, S. M. Gueret, O. Laita, R. J. Bland, I. A. Sutherland, I. K. Boddy and M. A. Brimble, Australian Journal of Chemistry, 2016, 69, 1268-1276. (IF = 1.6) https://doi.org/10.1071/CH16169
405. âSynthesis and Amylin Receptor Activity of Glycomimetics of Pramlintide using Click Chemistryâ L. R. Yule, R. L. Bower, H. Kaur, R. Kowalczyk, D. L. Hay and M. A. Brimble, Organic and Biomolecular Chemistry, 2016, 14, 5238-5245 (IF = 3.6) https://doi.org/10.1039/C6OB00850J
⢠(Invited article for âSelective Chemistry with Peptides and Proteinsâ themed issue edited by Professor Phil Dawson; Selected for âFront Coverâ)
404. âRadiation Damage and Racemic Crystallography Reveal the Unique Structure of the GASA/Snakin Protein Superfamilyâ H. Yeung, C. J. Squire, Y. Yosaatmadja, S. Panjikar, G. LĂłpez, A. Molina, E. N. Baker, P. W. R. Harris and M. A. Brimble, Angewandte Chemie International Edition, 2016, 55, 7930-7933. (IF = 11.3) https://doi.org/10.1002/anie.201602719
⢠(Selected for âFront Coverâ and as âVIP paperâ, < 5% of accepted papers receive this accolade; Featured in Chemistry in Australia, âElusive Potato Protein Structure Solved,â September issue 2016, p 11)
403. âReceptor Activity-Modifying Proteins 2 and 3 Generate Adrenomedullin Receptor Subtypes with Distinct Molecular Propertiesâ H. A. Watkins, M. Chakravarthy, R. S. Abhayawardana, J. J. Gingell, M. Garelja, M. Pardamwar, J. M. W. R. McElhinney, A. Lathbridge, A. Constantine, P. W. R. Harris, T.-Y. Yuen, M. A. Brimble, J. Barwell, D. R. Poyner, M. J. Woolley, A. C. Conner, A. A. Pioszak, C. A. Reynolds and D. L. Hay, Journal of Biological Chemistry, 2016, 291, 11657-11675. (IF = 4.6) https://doi.org/10.1074/jbc.m115.688218
402. âSynthesis and Structural Insight into ESX-1 Substrate Protein C, an Immunodominant Mycobacterium Tuberculosis-Secreted Antigenâ S. J. Son, P. W. R. Harris, C. J. Squire, E. N. Baker and M. A. Brimble, Biopolymers (Peptide Science), 2016, 106, 267-274. (IF = 2.9) https://doi.org/10.1002/bip.22838
401. âLipidation of Cysteine or Cysteine-Containing Peptides Using the Thiol-ene Reaction (CLipPA)â S.-H. Yang, P. W. R. Harris, G. M. Williams and M. A. Brimble, European Journal of Organic Chemistry, 2016, 33, 2608-2616. (IF = 3.1) https://doi.org/10.1002/ejoc.201501375
⢠(Selected for âFront Coverâ and as a âHot Topicsâ Article for all Wiley journals: http://www.wiley-vch.de/util/hottopics/clickchem/)
400. âA New High-Capacity Metal Ion-Complexing Gel Containing Cyclen Ligandsâ C. Dolan, F. Douret, D. C. Ware, P. J. Brothers, J. Jin, M. A. Brimble and D. Williams, RSC Advances, 2016, 6, 23645-23652. (IF = 3.8) https://doi.org/10.1039/C6RA00604C
399. âA Peptide Hydrogel Derived from a Fragment of Human Cardiac Troponin Câ L. M. De Leon-Rodriguez, M. Kamalov, Y. Hemar, A. K. Mitra, V. Castelletto, D. Hermida-Merino, I. W. Hamley and M. A. Brimble, Chemical Communications, 2016, 52, 4056-4059. (IF = 6.4) https://doi.org/10.1039/C6CC00209A
398. âFluorescent IGF-II Analogues for FRET-based Investigations into the Binding of IGF-II to the IGF-1Râ J. M. Cottam Jones, P. W. R. Harris, D. B. Scanlon, B. E. Forbes, M. A. Brimble and A. D. Abell, Organic and Biomolecular Chemistry, 2016, 14, 2698-2705. (IF = 3.6) https://doi.org/10.1039/C5OB02110C
397. âDivergent Reactivity via Cobalt Catalysis: An Epoxide Olefinationâ M. Jamieson, P. Hume, D. P. Furkert and M. A. Brimble, Organic Letters, 2016, 18, 468-471. (IF = 6.6) https://doi.org/10.1021/acs.orglett.5b03514
396. âA Convergent Synthesis of Gonytolide C Using an Intramolecular Oxa-Michael Additionâ F. F. Li, D. J. Atkinson, D. P. Furkert and M. A. Brimble, European Journal of Organic Chemistry, 2016, 33, 1145-1155. (IF = 3.3) https://doi.org/10.1002/ejoc.201501402
395. âThe Nedd4-1 WW Domain Recognizes the PY Motif Peptide through a Coupled Folding and Binding Equilibriumâ V. Panwalkar, P. Neudecker, M. Schmitz, J. Lecher, M. Schulte, K. Medini, M. Stoldt, M. A. Brimble, D. Willbold and A. Dingley, Biochemistry, 2016, 55, 659-674. (IF = 3.0) https://doi.org/10.1021/acs.biochem.5b01028
394. âEnantioselective Synthesis of BE Ring Analogues of Methyllycaconitineâ E. Dickson, L. I. Pilkington, M. A. Brimble and D. Barker, Tetrahedron, 2016, 72, 400-414. (IF = 2.6) https://doi.org/10.1016/j.tet.2015.11.057
393. âSynthesis and Activity of a Diselenide Bond Mimetic of the Antimicrobial Protein Caenopore-5â K. Medini, P. W. R. Harris, A. Menorca, K. Hards, G. M. Cook and M. A. Brimble, Chemical Science, 2016, 7, 2005-2010. (IF = 9.2) https://doi.org/10.1039/C5SC04187B
392. âElectrochemically-Controlled Grafting of Hydrophilic Brushes from Conducting Polymer Substratesâ L. T. Strover, J. MalmstrĂśm, L. Stubbing, M. A. Brimble and J. Travas-Sejdic, Electrochimica Acta, 2016, 188, 57-70. (IF = 4.5) https://doi.org/10.1016/j.electacta.2015.11.106
391. âTotal Synthesis and Structural Confirmation of the Antimalarial Naphthopyrone Lasionectrinâ V. L. Poral, D. P. Furkert and M. A. Brimble, Organic Letters, 2015, 17, 6214-6217. (IF = 6.7) https://doi.org/10.1021/acs.orglett.5b03202
390. âGlicentin-Related Pancreatic Polypeptide Inhibits Glucose-Stimulated Insulin Secretion from the Isolated Pancreas of Adult Male Ratsâ L. Whiting, K. W. Stewart, D. L. Hay, P. W. R. Harris, Y. S. Choong, A. R. J. Phillips, M. A. Brimble and G. J. S. Cooper, Physiological Reports, 2015, 3, e12638, 1-12. (IF = 2.13) https://doi.org/10.14814/phy2.12638
389. âPeptide Binding to a Bacterial Signal Peptidase Visualized by Peptide Tethering and Carrier-driven Crystallizationâ Y. T. Ting, P. W. R. Harris, G. Batot, M. A. Brimble, E. N. Baker and P. G. Young, International Union of Crystallography Journal (IUCrJ), 2016, 3, 10-19. (IF = 3.1) https://dx.doi.org/10.1107%2FS2052252515019971
388. âSynthesis of the Spiroketal Core of the Pinnatifinoside Family of Natural Productsâ D. F. Chorley, D. P. Furkert and M. A. Brimble, European Journal of Organic Chemistry, 2015, 32, 314-319. (IF = 3.3) https://doi.org/10.1002/ejoc.201501225
387. âFatty Acid Derived Pro-toxicants of the Rat Selective Toxicant Norbormideâ H. Choi, D. Conole, D. J. Atkinson, O. Laita, M. Jay-Smith, M. A. Pagano, G. Ribaudo, M. Cavalli, S. Bova, B. Hopkins, M. A. Brimble and D. Rennison, Chemistry and Biodiversity, 2016, 13, 762-775. (IF = 1.56) https://doi.org/10.1002/cbdv.201500241
386. âImproved Synthesis of the Unnatural Amino Acids AHMOD and AMD, Components of the Anticancer Peptaibol Culicinin Dâ K.-Y. Ko, S. Wagner, S.-H. Yang, D. P. Furkert and M. A. Brimble, Journal of Organic Chemistry, 2015, 80, 8631-8636. (IF = 4.6) https://doi.org/10.1021/acs.joc.5b01265
385. âImproved Strategy for the Synthesis of the Anticancer Agent Culicinin Dâ M. Stach, A. J. Weidkamp, S.-H. Yang, K.-Y Hung, D. P. Furkert, P. W. R. Harris, J. B. Smaill, A. V. Patterson and M. A. Brimble, European Journal of Organic Chemistry, 2015, 6341-6350. (IF = 3.3) https://doi.org/10.1002/ejoc.201500872
384. âNKT Cell-Dependent Glycolipid-Peptide Vaccines with Potent Anti-tumour Activityâ R. J. Anderson, B. J. Compton, C.-W Tang, A. Authier-Hall, C. M. Hayman, G. W. Swinerd, R. Kowalczyk, P. W. R. Harris, M. A Brimble, D. S. Larsen, O. Gasser, R. Weinkove, I. F. Hermans and G. F. Painter, Chemical Science, 2015, 6, 5120-5127. (IF = 9.2) https://doi.org/10.1039/C4SC03599B
⢠(Selected as an Edge Article and Front Cover)
383. âSynthesis of DOHNAA, a Mycobacterium tuberculosis Cholesterol CD Ring Catabolite and FadD3 Substrateâ L. A. Stubbing, J. S. Lott, S. S. Dawes, D. P. Furkert and M. A. Brimble, European Journal of Organic Chemistry, 2015, 6075-6083. (IF = 3.3) https://doi.org/10.1002/ejoc.201500698
382. âRegulation and Quality Control of Adiponectin Assembly by Endoplasmic Reticulum Chaperone ERp44â L. Hampe, M. Radjainia, C. Xu, P. W. R. Harris, G. Bashiri, D. C. Goldstone, M. A. Brimble, Y. Wang and A. K. Mitra, Journal of Biological Chemistry, 2015, 290, 18111-18123. (IF = 4.6) https://doi.org/10.1074/jbc.m115.663088
381. âConvergent Chemo-Enzymatic Synthesis of Mannosylated Glycopeptides; Targeting of Putative Vaccine Candidates to Antigen Presenting Cellsâ J. D. MacIntosh, M. A. Brimble, A. E. S. Brooks, P. R. Dunbar, R. Kowalczyk, Y. Tomabechi and A. J. Fairbanks, Chemical Science, 2015, 6, 4636-4642. (IF = 9.2) https://doi.org/10.1039/c5sc00952a
380. âCell-Targeted Platinum Nanoparticles and Nanoparticle Clustersâ S. Papst, M. A. Brimble, C. W. Evans, D. J. Verdon, V. Feist, P. R. Dunbar, R. D. Tilley and D. E. Williams, Organic and Biomolecular Chemistry, 2015, 13, 6567-6572. (IF = 3.6) https://doi.org/10.1039/C5OB00822K
379. âOn Resin Synthesis and Cross-linking of Collagen Peptides Containing the Advanced Glycation End-product Pyrraline via Maillard Condensationâ M. Kamalov, P. W. R. Harris, J. M. Wood and M. A. Brimble, Chemical Communications, 2015, 51, 9475-9478. (IF = 6.4) https://doi.org/10.1039/C5CC03052H
378. âStructural Basis for Receptor Activity-modifying Protein-Dependent Selective Peptide Recognition by a G protein-Coupled Receptorâ J. M. Booe, C. S. Walker, J. Barwell, G. Kuteyi, J. Simms, M. A. Jamaluddin, M. L. Warner, R. M. Bill, P. W. R. Harris, M. A. Brimble, D. R. Poyner, D. L. Hay and A. A. Pioszak, Molecular Cell, 2015, 58, 1040-1052. (IF = 15.3) https://doi.org/10.1016/j.molcel.2015.04.018
377. âDiabetes-Induced Alterations in Tissue Collagen and Carboxymethyllysine in Rat Kidneys: Association with Increased Collagen-degrading Proteinases and Amelioration by Cu(II)-selective Chelationâ S. Brings, S. Zhang, Y. S Choong, S. Hogl, M. Middleditch, M. Kamalov, M. A. Brimble, D. Gong and G. J. S. Cooper, Biochimica and Biophysica Acta (BBA) – Molecular Basis of Disease, 2015, 1852, 1610-1618. (IF = 5.1) https://doi.org/10.1016/j.bbadis.2015.04.014
376. âReplacement of the CysA7-CysB7 Disulfide Bond with a 1,2,3-Triazole Linker Causes Unfolding in Insulin Glargineâ G. M. Williams, K. Lee, X. Li, G. J. S. Cooper and M. A. Brimble, Organic and Biomolecular Chemistry, 2015, 13, 4059-4063. (IF = 3.6) https://doi.org/10.1039/C5OB00160A
375. âStudies Towards Development of Asymetric Double-Mannich Reactions of Chiral 2-Oxocyclohexanecarboxylate Derivatives with Bis(aminol)ethersâ K. J. Sparrow, S. Carley, T. SĂśhnel, D. Barker and M. A. Brimble, Tetrahedron, 2015, 71, 2210-2221. (IF = 2.8) https://doi.org/10.1016/j.tet.2015.02.083
374. âChemical Synthesis of a Polypeptide Backbone Derived from the Primary Sequence of the Cancer Protein NY-ESO-1 Enabled by Kinetically Controlled Ligation and Pseudoprolinesâ P. W. R. Harris and M. A. Brimble, Biopolymers (Peptide Science), 2015, 104, 116-127. (IF = 2.9) https://doi.org/10.1002/bip.22621
373. âSynthesis of the Spirocyclic Framework of Sesterterpenoid Natural Productsâ J. G. Hubert, D. P. Furkert and M. A. Brimble, Journal of Organic Chemistry, 2015, 80, 2715-2723. (IF = 4.8) https://doi.org/10.1021/jo502897u
⢠Highlighted by Douglas Taber in Organic Chemistry Highlights “Metal-Mediated C-C Ring Construction”: www.organic-chemistry.org/Highlights/2015/14December.shtm
372. âPreparation of cis-gamma-Hydroxycarvone Derivatives for Synthesis of Sesterterpenoid Natural Products: Total Synthesis of Phorbin Aâ J. G. Hubert, D. P. Furkert and M. A. Brimble, Journal of Organic Chemistry, 2015, 80, 2231-2239. (IF = 4.6) https://doi.org/10.1021/jo502748s
371. âPhysicochemical Studies on the Copper(II) Binding by Glycated Collagen Telopeptidesâ M. Kamalov, P. W. R. Harris, C. G. Hartinger, G. M. Miskelly, G. J. S. Cooper and M. A. Brimble, Organic and Biomolecular Chemistry, 2015, 13, 3058-3063. (IF = 3.6) https://doi.org/10.1039/C4OB02536A
370. âTotal Synthesis of the Cyclic Depsipeptide YM-280193, a Platelet Aggregation Inhibitorâ H. Kaur, P. W. R. Harris, P. J. Little and M. A. Brimble, Organic Letters, 2015, 17, 492-495. (IF = 6.3) https://doi.org/10.1021/ol503507g
369. âSynthesis of Novel Triazole-Containing Phosphonate Polymersâ C. Dolan, B. Naysmith, S. F. R. Hinkley, I. M. Sims, M. A. Brimble, D. E. Williams and J. Jin, Australian Journal of Chemistry, 2015, 68, 680-686. (IF = 1.6) https://doi.org/10.1071/CH14513
368. âUsing Mass Spectrometry to Detect, Differentiate and Semiquantitate Closely Related Peptide Hormones in Complex Milieu: Measurement of IGF-II and Vesiculinâ K. L. Lee, M. J. Middleditch, G. M. Williams, M. A. Brimble and G. J. S. Cooper, Endocrinology, 2015, 156, 1194-1199. (IF = 4.5) https://doi.org/10.1210/en.2014-1593
367. âSynthesis of the Antimicrobial S-Linked Glycopeptide, Glycocin Fâ M. A. Brimble, P. J. Edwards, P. W. R. Harris, G. E. Norris, M. L. Patchett, T. H. Wright, S.-H. Yang, and S. E. Carley, Chemistry â A European Journal, 2015, 21, 3556-3561. (IF = 5.7) https://doi.org/10.1002/chem.201405692
366. âChemical Synthesis of gamma-Secretase Activating Protein using Pseudo-glutamines as Ligation Sitesâ P. W. R. Harris, C. Squire, P. G. Young and M. A. Brimble, Biopolymers (Peptide Science), 2015, 104, 37-45. (IF = 2.9) https://doi.org/10.1002/bip.22600
365. âNeuroprotection with Glycine-2-Methylproline-Glutamate (G-2MePE) after Hypoxic-ischemic Brain Injury in Adult Rats,â S. Mathai, P. W. R. Harris, M. A. Brimble, A. J. Gunn and J. Guan, Journal of Experimental Stroke and Translational Medicine, 2015, 6, 1-11. An open access journal. https://www.openaccessjournals.com/articles/neuroprotection-with-glycine2methylprolineglutamate-g2mepe-after-hypoxicischemic-brain-injury-in-adult-rats-11896.html
364. âVirtual Screening for Novel Atg5-Atg16 Complex Inhibitors for Autophagy Modulationâ E. Robinson, E. Leung, A. M. Matuszek, N. Krogsgaard-Larsen, D. P. Furkert, M. A. Brimble, A. Richardson and J. Reynisson, MedChemComm, 2015, 6, 239-246. (IF = 2.7) https://doi.org/10.1039/C4MD00420E
363. âSynthesis of the Carbon Skeleton of the Griseorhodinsâ D. J. Atkinson, D. P. Furkert and M. A. Brimble, Tetrahedron, 2015, 71, 91-101. (IF = 2.8) https://doi.org/10.1016/j.tet.2014.11.030
362. âChemical Synthesis of a Pore-Forming Antimicrobial Protein, Caenopore-5, by Using Native Chemical Ligation at a Glu-Cys Site” K. Medini, P. W. R. Harris, K. Hards, A. J. Dingley, G. M. Cook and M. A. Brimble, ChemBioChem, 2015, 16, 328-336. (IF = 3.7) https://doi.org/10.1002/cbic.201402513
361. âFormal Synthesis of Nanaomycin D via a Hauser-Kraus Annulation Using a Chiral Enone-Lactoneâ
N. P. S. Hassan, B. J. Naysmith, J. Sperry and M. A. Brimble, Tetrahedron, 2015, 71, 7137-7143. (IF = 2.8) https://doi.org/10.1016/j.tet.2014.09.014
⢠(Invited Article for Tetrahedron Special Edition in memory of Professor Alan Katritzky)
360. âNonsymmetrical Azocarbonamide Carboxylates as Effective Mitsunobu Reagentsâ D. P. Furkert, B. Breitenbach, L. Juen, I. Sroka, M. Pantin and M. A. Brimble, European Journal of Organic Chemistry, 2014, 31, 7806-7809. (IF = 3.3) https://doi.org/10.1002/ejoc.201403152
359. âTotal Synthesis of the Macrocyclic N-Methyl Enamides Palmyrolide A and 2S-Sanctolide Aâ A. D. Wadsworth, D. P. Furkert and M. A. Brimble, Journal of Organic Chemistry, 2014, 79, 11179-11193. (IF = 4.6) https://doi.org/10.1021/jo502238r
358. âSynthesis and Evaluation of 9-Deoxy Analogues of (â)-Thysanone, an Inhibitor of HRV 3C Proteaseâ J. Y. Jeong, J. Sperry, J. A. Taylor and M. A. Brimble, European Journal of Medicinal Chemistry, 2014, 87, 220-227. (IF = 4.1) https://doi.org/10.1016/j.ejmech.2014.09.063
357. âProtecting-Group-Free One-pot Synthesis of Glycoconjugates Directly from Reducing Sugarsâ D. Lim, M. A. Brimble, R. Kowalczyk, A. J. A. Watson and A. J. Fairbanks, Angewandte Chemie International Edition, 2014, 53, 11907-11911. (IF = 13.7) https://doi.org/10.1002/anie.201406694
356. âSynthesis of the Revised Structure of Acortatarin Aâ H. M. Geng, L. A. Stubbing, J.L.-Y. Chen, D. P. Furkert and M. A. Brimble, European Journal of Organic Chemistry, 2014, 31, 6227-6241. (IF = 3.3) https://doi.org/10.1002/ejoc.201403000
355. âConvergent Chemoenzymatic Synthesis of a Library of Glycosylated Analogues of Pramlintide: Structure-Activity Relationships of Amylin Receptor Agonismâ R. Kowalczyk, M. A. Brimble, Y. Tomabechi, A. J. Fairbanks, M. Fletcher and D. L. Hay, Organic and Biomolecular Chemistry, 2014, 12, 8142-8151. (IF = 3.6) https://doi.org/10.1039/C4OB01208A
⢠(Selected for âFront Coverâ)
354. âToward an Asymmetric Synthesis of the Dimeric Pyranonaphthoquinone Antibiotic Crisamicin Aâ M. A. Brimble, N. P. S. Hassan, B. J. Naysmith and J. Sperry Journal of Organic Chemistry, 2014, 79, 7169-7178. (IF = 4.6) https://doi.org/10.1021/jo501344c
353. âAn Efficient Fmoc Solid-Phase Synthesis of an Amphiphile of the Neuroprotective Agent Glycyl-prolyl-glutamic acidâ P. W. R. Harris, G. T. Molenaar, Z. Amso, G. P. Savage and M. A. Brimble, Synlett, 2014, 25, 2221-2224. (IF = 2.7) https://doi.org/10.1055/s-0034-1378539
352. âTotal Synthesis of Virgatolide B via Exploitation of Intramolecular Hydrogen Bondingâ P. A. Hume, D. P. Furkert and M. A. Brimble, Journal of Organic Chemistry, 2014, 79, 5269-5281. (IF = 4.6) https://doi.org/10.1021/jo5008527
351. âSynthesis of Truncated Analogues of Preptin-(1-16), and Investigation of Their Ability to Stimulate Osteoblast Proliferationâ R. Kowalczyk, S. H. Yang, M. A. Brimble, K. E. Callon, M. Watson, Y.-E. Park and J. Cornish, Bioorganic and Medicinal Chemistry, 2014, 22, 3565-3572. (IF = 3.2) https://doi.org/10.1016/j.bmc.2014.05.026
350. âStructure and Activity of Streptococcus pyogenes SipA: A Signal Peptidase-Like Protein Essential for Pilus Polymerisationâ P. G. Young, T. Proft, P. W. R. Harris, M. A. Brimble and E. N. Baker, PLOS ONE, 2014, 9, e99135/1-e99135/13, 13 pp. (IF = 3.7) https://doi.org/10.1371/journal.pone.0099135
349. âExpedient Synthesis of Peptides Containing NÎľ-Carboxymethyllysineâ M. Kamalov, S. Yang, P. W. R. Harris, G. J. S. Cooper and M. A. Brimble, Synlett, 2014, 25, 1835-1838. (IF = 2.7) https://doi.org/10.1055/s-0033-1378305
348. âAn Investigation of the Role of the Adiponectin Variable Domain on the Stability of the Collagen-like Domainâ P. W. R. Harris, L. Hampe, M. Radjainia, M. A. Brimble and A. K. Mitra, Biopolymers (Peptide Science), 2014, 102, 313-321. (IF = 2.9) https://doi.org/10.1002/bip.22501
347. âSynthesis and Biological Evaluation of the Osteoblast Proliferating Cyclic Peptides Dianthins G and Hâ H. Kaur, A. M. Heapy, R. Kowalzcyk, Z. Amso, M. Watson, J. Cornish and M. A. Brimble, Tetrahedron, 2014, 70, 7788-7794. (IF = 2.8) https://doi.org/10.1016/j.tet.2014.04.035
⢠(Invited Article for Special Issue on Peptide Macrocycles)
346. âSite-Specific Cross-linking of Collagen Peptides by Lysyl Advanced Glycation Endproductsâ M. Kamalov, P. W. R. Harris, G. J. S. Cooper and M. A. Brimble, Chemical Communications, 2014, 50, 4944-4946. (IF = 6.4) https://doi.org/10.1039/C4CC02003K
345. âOne-Pot Synthesis of Functionalized Noble Metal Nanoparticles Using a Rationally Designed Phosphopeptideâ S. Papst, M. A. Brimble, R. D. Tilley, D. E. Williams, Particle and Particle Systems Characterization, 2014, 31, 971-975. https://doi.org/10.1002/ppsc.201300381
344. âSynthesis and Methemoglobinemia-inducing Properties of Benzocaine Isosteres Designed as Humane Rodenticidesâ D. Conole, T. M. Beck, M. Jay-Smith, M. D. Tingle, C. T. Eason, M. A. Brimble and D. Rennison, Bioorganic and Medicinal Chemistry, 2014, 24, 2220-2235. (IF = 3.1) https://doi.org/10.1016/j.bmc.2014.02.013
343. âPlant Antimicrobial Peptides Snakin-1 and Snakin-2: Chemical Synthesis and Insights into the Disulfide Connectivityâ P. W. R. Harris, S.-H Yang, A. Molina, G. LĂłpez, M. Middleditch and M. A. Brimble, Chemistry â A European Journal, 2014, 20, 5102-5110. (IF = 5.8) https://doi.org/10.1002/chem.201303207
342. âPreparation of Truncated Orf Virus Entry Fusion Complex Proteins by Chemical Synthesisâ H. Yeung, P. W. R. Harris, C. J. Squire, E. N. Baker and M. A. Brimble, Journal of Peptide Science, 2014, 20, 398-405. (IF = 2.1) https://doi.org/10.1002/psc.2627
341. âSynthesis of Highly Substituted Pyranonaphthalene Spiroketals Related to the Griseusins using a Hauser-Kraus Annulation Strategyâ B. J. Naysmith, D. P. Furkert and M. A. Brimble, Tetrahedron, 2014, 70, 1199-1206. (IF = 2.8) https://doi.org/10.1016/j.tet.2013.12.066
340. âA Convenient Method for the Asymmetric Synthesis of Fluorinated alpha-Amino Acids from Alcoholsâ F. Drouet, A. F. M. Noisier, C. S. Harris, D. P. Furkert and M. A. Brimble, European Journal of Organic Chemistry, 2014, 1195-1201. (IF = 3.3) https://doi.org/10.1002/ejoc.201301718
⢠(Selected for âFront Coverâ)
339. âSynthesis of the 2-Methylene Analogue of the HRV 3C Protease Inhibitor Thysanone (2-Carbathysanone)â K. SchĂźnemann, D. P. Furkert, E. C. Choi, S. Connelly, J. D. Fraser, J. Sperry and M. A. Brimble, Organic and Biomolecular Chemistry, 2014, 12, 905-912. (IF = 3.6) https://doi.org/10.1039/c3ob41951g
338. âTotal Synthesis of Heronapyrrole Câ X.-B. Ding, D. P. Furkert, R. J. Capon and M. A. Brimble, Organic Letters, 2014, 16, 378-381. (IF = 6.4) https://doi.org/10.1021/ol403246j
337. âSynthesis of the Spiroacetal Core of the Cephalosporolide Family of Natural Products, O. C. Finch, D. P. Furkert and M. A. Brimble, Tetrahedron, 2014, 70, 590-596. (IF = 2.8) https://doi.org/10.1016/j.tet.2013.12.012
336. âA Maillard Approach to 2-Formylpyrroles: Synthesis of Magnolamide, Lobechine and Funebralâ
T.-Z. Yuen, S. E. Eaton, T. M. Woods, D. P. Furkert, K. W. Choi and M. A. Brimble, European Journal of Organic Chemistry, 2014, 1431-1437. (IF = 3.3) https://doi.org/10.1002/ejoc.201301639
335. âIridium-Catalysed C-H Borylation Facilitates a Total Synthesis of the HRV 3C Protease Inhibitor (Âą)-Thysanoneâ K. SchĂźnemann, D. P. Furkert, S. Connelly, J. D. Fraser, J. Sperry and M. A. Brimble, Synlett, 2014, 25, 556-558. (IF = 2.7) https://doi.org/10.1055/s-0033-1340495
334. âAn Important Side Reaction Using the Thiol, 3,6-Dioxa-1,8-octanedithiol (DODT), in 9-Fluorenylmethoxycarbonyl Based Solid Phase Peptide Synthesisâ P. W. R. Harris, R. Kowalczyk, S.-H. Yang, G. M. Williams and M. A. Brimble, Journal of Peptide Science, 2014, 20, 186-190. (IF = 2.1) https://doi.org/10.1002/psc.2595
333. âTotal Chemical Synthesis of an Orf Virus Protein, ORFV002, an Inhibitor of the Master Gene Regulator NF-ďŤBâ S. J. Son, P. W. R. Harris, C. J. Squire, E. N. Baker and M. A. Brimble, Biopolymers (Peptide Science), 2014, 102, 137-144. (IF = 2.9) https://doi.org/10.1002/bip.22445
332. âSynthesis and Biological Evaluation of 7-Deoxy Analogues of the Human Rhinovirus 3C Protease Inhibitor Thysanoneâ K. SchĂźnemann, D. P. Furkert, S. Connelly, J. D. Fraser, J. Sperry and M. A. Brimble, European Journal of Organic Chemistry, 2014, 122-128. (IF = 3.3) https://doi.org/10.1002/ejoc.201301515
331. âSynthesis of a Novel Polyaniline Glycopolymer and its Lectin Binding Studiesâ C. Wilcox, J. Jin, H. Charville, S. Swift, T. To, P. A. Kilmartin, C. W. Evans, R. Cooney and M. A. Brimble, Australian Journal of Chemistry, 2014, 67, 562-569. (IF = 1.9) https://doi.org/10.1071/CH13452
330. âStructure-Activity Relationships of the N-Terminus of Calcitonin Gene-related Peptide: Key Roles of Alanine-5 and Threonine-6 in Receptor Activationâ D. L. Hay, P. W. R. Harris, R. Kowalczyk, M. A. Brimble, D. L. Rathbone, J. Barwell, A. C. Conner and D. R. Poyner, British Journal of Pharmacology, 2014, 171, 415-426. (IF = 5.1) https://dx.doi.org/10.1111%2Fbph.12464
329. âSynthesis of an Azido Precursor (2S,5R)-5-Hydroxylysine Using an Asymmetric Organocatalytic Chlorination/Reduction Sequenceâ M. Johannes and M. A. Brimble, Journal of Organic Chemistry, 2013, 79, 12809-12813. (IF = 4.6) https://doi.org/10.1021/jo402220s
328. âSynthesis of Leptosin, A Glycoside Isolated from Manuka Honeyâ H. R. M. Aitken, M. Johannes, K. M. Loomes and M. A. Brimble, Tetrahedron Letters, 2013, 54, 6916-6919. (IF = 2.7) https://doi.org/10.1016/j.tetlet.2013.10.042
⢠(Selected for âFront Coverâ)
327. âSynthesis and Methemoglobinemia-inducing Properties of Analogues of para-aminopropiophenone Designed as Humane Rodenticidesâ D. Rennison, D. Conole, M. D. Tingle, J. Yang , C. T. Eason and M. A. Brimble, Bioorganic and Medicinal Chemistry Letters, 2013, 23, 6629-6635. (IF = 2.5) https://doi.org/10.1016/j.bmcl.2013.10.046
326. âSynthesis and Cytotoxicity of Pyranonaphthoquinone Natural Product Analogues Under Bioreductive Conditionsâ A. M. Heapy, A. V. Patterson, J. B. Smaill, S. M. F. Jamieson, C. P. Guise, J. Sperry, P. A. Hume, K. Rathwell and M. A. Brimble, Bioorganic and Medicinal Chemistry, 2013, 21, 7971-7980. (IF = 2.9) https://doi.org/10.1016/j.bmc.2013.09.052
325. âTotal Synthesis of Virgatolide Bâ P. A. Hume, D. P. Furkert and M. A. Brimble, Organic Letters, 2013, 15, 4588-4591. (IF = 6.3) https://doi.org/10.1021/ol402191t
324. âSynthesis of Benzannulated Spiroacetals using Chiral Gold-Phosphine Complexes and Chiral Anionsâ R. Quach, D. P. Furkert and M. A. Brimble, Tetrahedron Letters, 2013, 54, 5865-5868. (IF = 2.7) https://doi.org/10.1016/j.tetlet.2013.08.077
323. âDirect Peptide Lipidation through Thiol-ene Coupling Enables Rapid Synthesis and Evaluation of Self-adjuvanting Vaccine Candidatesâ T. H. Wright, A. E. S. Brooks, A. J. Didsbury, G. M. Williams, P. W. R. Harris, R. P. Dunbar and M. A. Brimble, Angewandte Chemie International Edition, 2013, 52, 10616-10619. (IF = 13.7) https://doi.org/10.1002/anie.201305620
322. âNovel Preparation of Chiral alpha-Amino Acids using the MitsunobuâTsunoda Reactionâ A. F. M. Noisier, C. S. Harris and M. A. Brimble, Chemical Communications, 2013, 49, 7744-7746. (IF = 6.4) https://doi.org/10.1039/C3CC44717K
321. âThe Synthesis and Lectin-Binding Properties of Novel Mannose-Functionalised Polymersâ H. Charville, J. Jin, C. W. Evans, M. A. Brimble and D. E. Williams, Royal Society of Chemistry Advances, 2013, 3, 15435-15441. (IF = 2.6) https://doi.org/10.1039/C3RA42781A
320. âEnantioselective Access to Benzannulated Spiroketals using a Chiral Sulfoxide Auxiliaryâ H. R. M. Aitken, D. P. Furkert, J. G. Hubert, J. M. Wood and M. A. Brimble, Organic and Biomolecular Chemistry, 2013, 11, 5147-5155. (IF = 3.6) https://doi.org/10.1039/C3OB41065J
319. âAn Improved Method for the Synthesis of Lipopeptide TLR2-Agonists Using Click Chemistryâ T. H. Wright, A. E. S. Brooks, A. J. Didsbury, J. D. McIntosh, K. Burkert, H. Yeung, G. M. Williams, P. R. Dunbar and M. A. Brimble, Synlett, 2013, 24, 1835-1841. (IF = 2.7) https://doi.org/10.1055/s-0033-1339349
318. âProdrugs of N-Dicarboximide Derivatives of the Rat Selective Toxicant Norbormideâ D. Rennison, O. Laita D. Conole, M. Jay-Smith, J. Knauf, S. Bova, M. Cavalli, B. Hopkins, D. S. Linthicum and M. A. Brimble, Bioorganic and Medicinal Chemistry, 2013, 21, 5886-5899. (IF = 2.9) https://doi.org/10.1016/j.bmc.2013.06.071
317. âChemical Synthesis of a Masked Analogue of the Fish Antifreeze Potentiating Protein (AFPP)â S.-H. Yang, J. M. Wojnar, P. W. R. Harris, A. L. DeVries, C. W. Evans and M. A. Brimble, Organic and Biomolecular Chemistry, 2013, 11, 4935-4942. (IF = 3.6) https://doi.org/10.1039/C3OB41066H
⢠(Featured in Chemeurope and Bionity: http://www.chemeurope.com/en/news/144123/; www.bionity.com/en/news/144123/ and in âChemistry Worldâ Sept. 2013, p.29, http://www.rsc.org/chemistryworld/2013/07/antifreeze-fish-protein-synthesis)
316. âSynthesis of the Cysteine Protease Inhibitors CPI-2081a and CPI-2081b Using a Controlled SPPS Byproduct Forming Reactionâ A. M. Heapy, M. Dragunow and M. A. Brimble, Synlett, 2013, 24, 1818-1824. (IF = 2.7) https://doi.org/10.1055/s-0033-1339347
315. âGrafting from Poly(3,4-ethylenedioxythiophene): A Simple Route to Versatile Electrically Addressable Surfacesâ J. MalmstrĂśm, M. K. Nieuwoudt, L. T. Strover, A. Hackett, O. Laita, M. A. Brimble, D. E. Williams and J. Travas-Sejdic, Macromolecules, 2013, 46, 4955-4965. (IF = 5.5) https://doi.org/10.1021/ma400803j
314. âStructure and Dynamics of Human Nedd4-1 WW3 in Complex with the alphaENaC PY Motifâ R. Bobby, K. Medini, P. Neudecker, T. V. Lee, M. A. Brimble, F. J. McDonald, J. S. Lott and A. J. Dingley, Biochimica et Biophysica Acta – Proteins and Proteomics, 2013, 1834, 1632-1641. (IF = 3.6) https://doi.org/10.1016/j.bbapap.2013.04.031
313. âSynthesis of Stable Isotope Labelled Monolysyl Advanced Glycation Endproductsâ T. M. Woods, G. S. Cooper and M. A. Brimble, Amino Acids, 2013, 45, 319-325. (IF = 3.9) https://doi.org/10.1007/s00726-013-1498-9
312. âOne-Pot Synthesis of Water Soluble Iron Nanoparticles Using Rationally Designed Peptides and Ligand Releaseâ S. Papst, S. Cheong, M. J. Banholzer, M. A. Brimble, D. E. Williams and R. D. Tilley, Chemical Communications, 2013, 49, 4540-4542. (IF = 6.4) https://doi.org/10.1039/C3CC41751D
311. âSynthesis of the Griseusin B Framework via a one-pot Annulation-Methylation-Double Deprotection-Spirocyclisation Sequenceâ B. J. Naysmith and M. A. Brimble, Organic Letters, 2013, 15, 2006-2009. (IF = 6.3) https://doi.org/10.1021/ol400686f
310. âSynthesis of the IGF-II-like Hormone Vesiculin using Regioselective Formation of Disulfide Bondsâ G. M. Williams, G. J. S. Cooper, K. Lee, L. Whiting, and M. A. Brimble, Organic and Biomolecular Chemistry, 2013, 11, 3145-3150. (IF = 3.6) https://doi.org/10.1039/C3OB40322J
309. âTelomerase Inhibition Studies of Novel Spiroketal-Containing Rubromycin Derivativesâ T.-Y. Yuen, Y.-P. Ng, F. C. F. Ip, J. L.-Y. Chen, D. J. Atkinson, J. Sperry, N. Y. Ip and M. A. Brimble, Australian Journal of Chemistry, 2013, 66, 530-533. (IF = 2.1) https://doi.org/10.1071/CH13035
308. âTotal Synthesis of Chaetoquadrins H and Iâ U. B. Kim, A. F. Dalebrook, D. P. Furkert and M. A. Brimble, Synlett, 2013, 723-726. (IF = 2.7) https://doi.org/10.1055/s-0032-1318333
307. âA Comparison of Boc and Fmoc SPPS Strategies for the Preparation of C-Terminal Peptide alpha-Thioesters: NY-ESO-1 39Cys-68Ala-COSRâ P. W. R. Harris and M. A. Brimble, Biopolymers (Peptide Science), 2013, 100, 356-365. (IF = 2.9) https://doi.org/10.1002/bip.22223
306. âSynthesis of a 6,6-Spiroketal Amino Acid and its Incorporation into a Peptide Turn Sequence using Solid Phase Peptide Synthesisâ J. T. B. Kueh, K. W. Choi, G. M. Williams, K. Moehle, B. Bacsa, J. A. Robinson and M. A. Brimble, Chemistry â A European Journal, 2013, 19, 3807-3811. (IF = 5.8) https://doi.org/10.1002/chem.201204546
305. âIdentification of Key Residues Involved in Adrenomedullin Binding to the AM1 Receptorâ H. A. Watkins, M. Au, R. Bobby, J. K. Archibold, N. Abdul-Manan, J. M. Moore, M. J. Middleditch, G. M. Williams, M. A. Brimble, A. J. Dingley and D. L. Hay, British Journal of Pharmacology, 2013, 169, 143-155. (IF = 5.1) https://doi.org/10.1111/bph.12118
304. âTotal Synthesis of Chaetoquadrins A-Câ U. B. Kim, D. P. Furkert and M. A. Brimble, Organic Letters, 2013, 15, 658-661. (IF = 6.3) https://doi.org/10.1021/ol303482k
303. âA New Precursor for Conducting Polymer-based Brush Interfaces with Electroactivity in Aqueous Solutionâ
L. T. Strover, J. MalmstrĂśm, O. Laita, J. Reynisson, N. Aydemir, M. K. Nieuwoudt, D. E. Williams, P. R. Dunbar, M. A. Brimble and J. Travas-Sejdic, Polymer, 2013, 54, 1305-1317. (IF = 3.4) https://doi.org/10.1016/j.polymer.2012.11.083
302. âDNA Adduct Formation of Mitomycin C. A Test Case for DFT Calculations on Model Systemsâ P. Hume, M. A. Brimble and J. Reynisson, Computational and Theoretical Chemistry, 2013, 1005, 9-15. (IF = 1.4) http://dx.doi.org/10.1016/j.comptc.2012.10.022
301. âNatural Product-inspired Pyranonaphthoquinone Inhibitors of Indoleamine 2,3-Dioxygenase (IDO-1)â D. J. A. Bridewell, J. Sperry, J. R. Smith, P. Kosim-Satyaputra, L.-M. Ching, J. F. Jamie and M. A. Brimble, Australian Journal of Chemistry, 2013, 66, 40-49. https://doi.org/10.1071/CH12393
300. âSynthesis and Self-Assembly of a Peptide-Amphiphile as a Drug Delivery Vehicleâ S. J. Son, M. A. Brimble, S. Yang, P. W. R. Harris, T. Reddingius, B. W. Muir, O. E. Hutt, L. Waddington, J. Guan, and G. P. Savage, Australian Journal of Chemistry, 2013, 66, 23-29. (IF = 1.9) https://doi.org/10.1071/CH12347
⢠(Selected for âfront coverâ)
299. âSynthesis of the Tetracyclic Core of Berkelic Acid using Gold(I)-Catalyzed Hydroarylation and Oxidative Radical Cyclizationsâ M. A. Brimble, I. Haym, J. Sperry and D. P. Furkert, Organic Letters, 2012, 14, 5820-5823. (IF = 6.1) https://doi.org/10.1021/ol302536j
298. âSynthesis of the Peptaibol Framework of the Anticancer Agent Culicinin D: Stereochemical Assignment of the AHMOD Moietyâ K.-Y. Hung, P. W. R. Harris and M. A. Brimble, Organic Letters, 2012, 14, 5784-5787. (IF = 6.1) https://doi.org/10.1021/ol302852q
297. âSynthesis of Monolysyl Advanced Glycation Endproducts and Their Incorporation into Collagen Model Peptidesâ T. Woods, M. Kamalov, P.W. R. Harris, G. J. S. Cooper and M. A. Brimble, Organic Letters, 2012, 14, 5740-5743. (IF = 6.1) https://doi.org/10.1021/ol302745f
296. âTotal Synthesis of the Initially Reported and Revised Structures of the Neuroprotective Agent Palmyrolide Aâ A. D. Wadsworth, D. P. Furkert, J. Sperry and M. A. Brimble, Organic Letters, 2012, 14, 5374-5377. (IF = 6.1) https://doi.org/10.1021/ol3025956
295. âTotal Synthesis of 7′,8′-Dihydroaigialospirolâ T. Y. Yuen and M. A. Brimble, Organic Letters, 2012, 14, 5154-5157. (IF = 6.1) https://doi.org/10.1021/ol302498v
294. âHow to Blast Osteoblasts? Novel Dicarba Analogues of Amylin-(1-8) to Treat Osteoporosisâ R. Kowalczyk, M. A. Brimble, K. E. Callon, M.Watson and J. Cornish, Bioorganic and Medicinal Chemistry, 2012, 20, 6011-6018. (IF = 2.9) https://doi.org/10.1016/j.bmc.2012.08.053
⢠(highlighted in World Biomedical Frontiers<http://biomedfrontiers.org/ [ISSN: 2328-0166])
293. âA Single Pseudoproline and Microwave Solid Phase Peptide Synthesis Facilitates an Efficient Synthesis of Human Amylin 1-37″ P. W. R. Harris, R. Kowalczyk, D. Hay and M. A. Brimble, International Journal of Peptide Research and Therapeutics, 2013, 19, 147-155. (IF = 1.3) https://doi.org/10.1007/s10989-012-9325-9
292. âSynthesis of Multivalent Neoglycoconjugates of MUC1 by the Conjugation of Carbohydrate-centred, Triazole-linked Glycoclusters to MUC1 peptides using Click Chemistryâ D. J. Lee, S.-H. Yang, G. M. Williams and M. A. Brimble, Journal of Organic Chemistry, 2012, 77, 7564-7571. (IF = 4.6) https://doi.org/10.1021/jo3013435
291. âA Slow Gradient Approach for the Purification of Synthetic Polypeptides by Reversed Phase High Performance Liquid Chromatographyâ P. W. R. Harris, D. J. Lee and M. A. Brimble, Journal of Peptide Science, 2012, 18, 549-555. (IF = 2.1) https://doi.org/10.1002/psc.2432
290. âSynthesis and SAR of a Library of Cell-Permeable Biotin-R8ERY* Peptidomimetics Inhibiting alpha4 beta7 Integrin Mediated Adhesion of TK-1 Cells to MAdCAM-1-Fcâ S. Papst, A. F. M. Noisier, M. A. Brimble, Y. Yang, Y.-C. Chan and G. W. Krissansen, Australian Journal of Chemistry, 2012, 65, 1349-1358. (IF = 1.9) http://dx.doi.org/10.1071/CH12227
289. âSynthesis and Biological Evaluation of Tyrosine Modified Analogues of the alpha4 beta7 Integrin Inhibitor Biotin-R8ERYâ S. Papst, A. F. M. Noisier, M. A. Brimble, Y. Yang and G. W. Krissansen, Bioorganic and Medicinal Chemistry, 2012, 20, 5139-5149. (IF = 2.9) https://doi.org/10.1016/j.bmc.2012.07.010
288. âSynthesis of the All-L Cyclopeptides Versicoloritides A, B and Câ H. Kaur, A. M. Heapy and M. A. Brimble, Synlett, 2012, 23, 2284-2288. (IF = 2.7) https://doi.org/10.1055/s-0032-1316994
287. âA Simple Solid Phase, Peptide-based Fluorescent Assay for the Efficient and Universal Screening of HRV 3C Protease Inhibitorsâ K. SchĂźnemann, S. Connelly, R. Kowalczyk, J. Sperry, I. A. Wilson, J. D. Fraser and M. A. Brimble, Bioorganic and Medicinal Chemistry Letters, 2012, 22, 5018-5024. (IF = 2.5) https://doi.org/10.1016/j.bmcl.2012.06.015
286. âA Tandem Diels-Alder/Mannich Approach to the Synthesis of AE and ABE Ring Analogues of Delphinium Alkaloidsâ K. J. Goodall, M. A. Brimble and D. Barker, Tetrahedron, 2012, 68, 5759-5778. (IF = 2.8) https://doi.org/10.1016/j.tet.2012.05.037
285. âDesign and Synthesis of Prodrugs of the Rat Selective Toxicant Norbormideâ D. Rennison, O. Laita, S. Bova, M. Cavalli, B. Hopkins, D. S. Linthicum and M. A. Brimble, Bioorganic and Medicinal Chemistry, 2012, 20, 3997-4011. (IF = 2.9) https://doi.org/10.1016/j.bmc.2012.05.014
284. âAccess to 2-Alkyl Chromanones via a Conjugate Addition Approachâ L. A. Stubbing, F. F. Li, D.P. Furkert, V. E. Caprio and M. A. Brimble, Tetrahedron, 2012, 68, 6948-6956. (IF = 2.8) https://doi.org/10.1016/j.tet.2012.05.115
283. âDetermination of pKa and Forced Degradation of the Indoloquinoline Antimalarial Compound Cryptolepine
Hydrochlorideâ N. Kuntworbe, M. A. Brimble, R. G. Alany and R. Al-Kassas, Pharmaceutical Development and Technology, 2013, 18, 866-876. (IF = 1.3) https://doi.org/10.3109/10837450.2012.668554
281. âRegioselective Iridium(I)-Catalysed Remote Borylation of Oxygenated Naphthalenesâ P. Hume, D. P. Furkert and M.A. Brimble, Tetrahedron Letters, 2012, 53, 3771-3773. (IF = 2.7) https://doi.org/10.1016/j.tetlet.2012.05.040
280. âNovel Phosphopeptides as Surface-Active Agents in Iron Nanoparticle Synthesisâ R. Peltier, W. R. Siah, G. V. M. Williams, M. A. Brimble, R. D. Tilley and D. E. Williams, Australian Journal of Chemistry, 2012, 65, 680-685. (IF = 1.9) https://doi.org/10.1071/CH12168
279. âA Highly Conserved Tryptophan in the N-Terminal Variable Domain Regulates Rate of Disulfide Bond Formation and Oligomeric Assembly of Adiponectinâ M. Radjainia, B. Huang, B. Bai, M. Schmitz, S. H. Yang, P. W. R. Harris, M. D. W. Griffin, M. A. Brimble, Y. Wang, and A. M. Mitra, FEBS Journal, 2012, 279, 2495-2507. (IF = 4.3) https://doi.org/10.1111/j.1742-4658.2012.08630.x
278. âA Method for the Generation of Pam2Cys-Based Lipopeptide Mimics via CuAAC Click Chemistryâ H. Yeung, D. J. Lee, G. M. Williams, P. W. R. Harris and M. A. Brimble, Synlett, 2012, 23, 1617-1620. (IF = 2.7) https://doi.org/10.1055/s-0031-1291148
277. âTyrosine Modified Analogues of the alpha4 beta7 Integrin Inhibitor Biotin-R8ERY Prepared via Click Chemistry: Synthesis and Biological Evaluationâ S. Papst, A. Noisier, M. A. Brimble, Y. Yang and G. W. Krissansen, Bioorganic and Medicinal Chemistry, 2012, 20, 2638-2644. (IF = 2.9) https://doi.org/10.1016/j.bmc.2012.02.035
⢠(Selected for inclusion on Global Medical Discovery Website; http://globalmedicaldiscovery.com)
276. âSynthesis and Evaluation of Disulfide Bond Mimetics of Amylin-(1-8) as Agents to Treat Osteoporosisâ R. Kowalczyk, P. W. R. Harris, M. A. Brimble, K. E. Callon, M. Watson and J. Cornish, Bioorganic and Medicinal Chemistry, 2012, 20, 2661-2668. (IF = 2.9) https://doi.org/10.1016/j.bmc.2012.02.030
275. âThe Bioreductive Alkylation of DNA by Kalafungin. A Theoretical Investigationâ P. Hume, J. Reynisson and M. A. Brimble, Australian Journal of Chemistry, 2012, 65, 402-408. (IF = 1.9) https://doi.org/10.1071/CH12018
274. âA Convergent Synthesis of the 2-Formylpyrrole Spiroketal Natural Product Acortatarin Aâ H. M. Geng, J. L.-Y. Chen, D. P. Furkert, S. Jiang and M. A. Brimble, Synlett, 2012, 23, 855-858. (IF = 2.7) https://doi.org/10.1055/s-0031-1290508
273. âSynthesis and anti-Helicobacter pylori Activity of Analogues of Spirolaxine Methyl Etherâ I. Dimitrov, D. P. Furkert, J. D. Fraser, F. J. Radcliff, O. Finch and M. A. Brimble, MedChemComm, 2012, 3, 944-949. (IF = 2.7) https://doi.org/10.1039/C2MD00314G
⢠(Invited paper for Special Issue on Natural Products and selected for Front Cover)
272. âSynthesis of a Dicarba Analogue of Human beta-Defensin-1 using a Combined Ring Closing Metathesis-Native Chemical Ligation Strategyâ A. M. Heapy, G. M. Williams, J. D. Fraser and M. A. Brimble, Organic Letters, 2012, 14, 878-881. (IF = 6.1) https://doi.org/10.1021/ol203407z
271. âMetabolic and Behavioural Adaptations During Early Development of the Antarctic Silverfish, Pleuragramma Antarcticumâ C. Evans, D. E. Williams, M. Vacchi, M. A. Brimble and A. L. DeVries, Polar Biology, 2012, 35, 891-898. (IF = 1.7) http://dx.doi.org/10.1007/s00300-011-1134-7
270. âAn Efficient Synthesis of 3-Alkyl-1,5,3-dioxazepanes and Their Use as Electrophiles in Double Mannich Reactionsâ K. Sparrow, D. Barker and M.A. Brimble, Tetrahedron, 2012, 68, 1017-1028. (IF = 2.8) https://doi.org/10.1016/j.tet.2011.11.090
269. âEnantioselective Synthesis of C-Linked Spiroacetal-Triazoles as Privileged Natural Product-like Scaffoldsâ J. T. B. Kueh, K. W. Choi and M. A. Brimble, Organic and Biomolecular Chemistry, 2012, 10, 5993-6002. (IF = 3.6) https://doi.org/10.1039/C2OB06802H
⢠(Invited paper for Special Issue to celebrate 10th Anniversary of OBC)
268. âSynthesis of the Antifungal Cyclic Peptides Tunicyclins C and Dâ H. Kaur, A. M. Heapy and M. A. Brimble, Synlett, 2012, 23, 275-277. (IF = 2.7) https://doi.org/10.1055/s-0031-1290071
267. âFormal Synthesis of Berkelic Acid: A Lesson in alpha-Alkylation Chemistryâ M. McLeod, Z. Wilson and M. A. Brimble, Journal of Organic Chemistry, 2012, 77, 400-406. (IF = 4.6) https://doi.org/10.1021/jo201988m
266. âTotal Synthesis of Danshenspiroketallactoneâ D. F. Chorley, J. L.-Y. Chen, D. P. Furkert, J. Sperry and M. A. Brimble, Synlett, 2012, 23, 128-130. (IF = 2.7) https://doi.org/10.1055/s-0031-1290082
265. âThe Chemical Synthesis of the Collagenous Domain of the Hormone Adiponectinâ P. W. H. Harris and M. A. Brimble, International Journal of Peptide Research and Therapeutics, 2012, 18, 63-70. (IF = 1.3) https://doi.org/10.1007/s10989-011-9279-3
264. âSynthesis and Recycling of Antifreeze Glycoproteins in Polar Fishesâ C. W. Evans, L. Hellman, M. Middleditch, J. M. Wojnar, M. A. Brimble and A. L. DeVries, Antarctic Science, 2012, 24, 259-268. (IF = 1.6) https://doi.org/10.1017/S0954102012000119
263. âSynthesis of the Bis-Spiroacetal Core of the Antimitotic Agent Spirastrellolideâ J. L.-Y. Chen and M. A. Brimble, Journal of Organic Chemistry, 2011, 76, 9417-9428. (IF = 4.6) https://doi.org/10.1021/jo201729t
262. âSynthesis of a NDPK Phosphocarrier Domain Peptide Containing a Triazolylalanine Analogue of Phosphohistidine Using Click Chemistryâ S.-H. Yang, D.-J. Lee and M. A. Brimble, Organic Letters, 2011, 13, 5604-5607. (IF = 5.9) https://doi.org/10.1021/ol202333u
261. âAn Enantioselective Formal Synthesis of Berkelic Acidâ M. C. McLeod, Z. E. Wilson and M. A. Brimble, Organic Letters, 2011, 13, 5382-5385. (IF = 5.9) https://doi.org/10.1021/ol202265g
260. âAn Improved Procedure for the Preparation of Aminomethyl Polystyrene Resin and its use in Solid Phase (Peptide) Synthesisâ P. W. R. Harris, S.-H. Yang and M. A. Brimble, Tetrahedron Letters, 2011, 52, 6024-6026. (IF = 2.7) https://doi.org/10.1016/j.tetlet.2011.09.010
259. âThe Translocator Protein (Peripheral Benzodiazepine Receptor) Mediates Rat-selective Activation of the Mitochondrial Permeability Transition by Norbormideâ A. Zulian, J. Ĺ ileikytÄ, V. Petronilli, S. Bova, F. Dabbeni-Sala, G. Cargnelli, D. Rennison, M. A. Brimble, B. Hopkins, P. Bernardi and F. Ricchelli, Biochimica et Biophysica Acta â Bioenergetics, 2011, 1807, 1600-1605. (IF = 4.8) https://doi.org/10.1016/j.bbabio.2011.08.007
258. âThe Enantioselective Synthesis of Tetracyclic Methyllycaconitine Analoguesâ K. Sparrow, D. Barker and M. A. Brimble, Tetrahedron, 2011, 67, 7989-7999. (IF = 2.8) https://doi.org/10.1016/j.tet.2011.08.026
257. âGold(I)-Catalysed Intramolecular Hydroamination of alpha-Quaternary Alkynes: Synthetic Studies Towards Spiroimine Marine Toxinsâ Y. C. Zhang, D. P. Furkert, S. Gueret, F. Lombard and M. A. Brimble, Tetrahedron Letters, 2011, 4896-4898. (IF = 2.7) https://doi.org/10.1016/j.tetlet.2011.07.048
256. âTotal Synthesis of Paecilospironeâ T.-Y. Yuen, S.-H. Yang and M. A. Brimble, Angewandte Chemie International Edition, 2011, 50, 8350-8353. (IF = 13.5) http://dx.doi.org/10.1002/anie.201103117
255. âEnantioselective Synthesis of Pyranonaphthoquinone Antibiotics using a CBS Reduction/Cross-Metathesis/oxa-Michael Strategyâ P. A. Hume, J. Sperry and M. A. Brimble, Organic and Biomolecular Chemistry, 2011, 9, 5423-5430. (IF = 3.7) http://dx.doi.org/10.1039/c1ob05595j
254. âA Flexible Approach to 6,5-Benzannulated Spiroketalsâ Z. E. Wilson, J. G. Hubert and M. A. Brimble, European Journal of Organic Chemistry, 2011, 28, 3938-3945. (IF = 3.3) http://dx.doi.org/10.1002/ejoc.201100345
⢠(Invited Paper for Special Issue to Celebrate International Year of Chemistryâ)
253. âEfficient Synthesis of the Spiroacetal Core of Paecilospirone via Oxidative Radical Cyclisationâ M. Jay-Smith, D. P. Furkert, J. Sperry and M. A. Brimble, Synlett, 2011, 1395-1398. (IF = 2.7) http://dx.doi.org/10.1055/s-0030-1260564
252. âSynthesis of Benzannulated Spiroketals using an Oxidative Radical Cyclizationâ J. Sperry, Y.-C. Liu, Z. E. Wilson, J. G. Hubert and M. A. Brimble, Synthesis, 2011, 1383-1398. (IF = 2.5) http://dx.doi.org/10.1055/s-0030-1259981
251. âSynthesis of an Isotopically-Labelled Antarctic Fish Antifreeze Glycoprotein Probeâ J. M. Wojnar, C. W. Evans, A. L. DeVries and M. A. Brimble, Australian Journal of Chemistry, 2011, 64, 723-731.(IF = 1.9) https://doi.org/10.1071/CH10464
⢠(Invited paper for Special Issue on Women in Science to celebrate International Year of Chemistry and 100th Anniversary of Nobel Prize being awarded to Marie Curie)
250. âSynthesis of MUC1 Neoglycopeptides using Efficient Microwave-Enhanced Chaotrope-Assisted Click Chemistryâ D. J. Lee, P. W. R. Harris and M. A. Brimble, Organic and Biomolecular Chemistry, 2011, 9, 1621-1626. (IF = 3.6) https://doi.org/10.1039/C0OB01043J
249. âSynthesis and Assignment of Stereochemistry of the Antibacterial Cyclic Peptide Xenamatideâ K.-Y. Hung, P. W. R. Harris, A. M. Heapy and M. A. Brimble, Organic and Biomolecular Chemistry, 2011, 9, 236-242. (IF = 3.6) https://doi.org/10.1039/C0OB00315H
248. âA Convergent Synthesis of the [4.4]-Spiroacetal-Îł-lactones Cephalosporolides E and Fâ M. A. Brimble, O. C. Finch, A. M. Heapy, J. D. Fraser, D. P. Furkert and P. D. OâConnor, Tetrahedron, 2011, 67, 995-1001. (IF = 2.8) https://doi.org/10.1016/j.tet.2010.11.107
247. âSynthesis of Benzotriazole Analogues of the Helicobactericidal Agents CJ-13,015, CJ-13,102, CJ-13,108 and CJ-13,104 using a Regioselective 1,3-Dipolar Cycloadditionâ D. J. Atkinson, J. Sperry and M. A. Brimble, Synlett, 2011, 99-103. (IF = 2.7) http://dx.doi.org/10.1055/s-0030-1259081
246. âHow do Antarctic Notothenioid Fishes Cope with Internal Ice? A Novel Function for Antifreeze Glycoproteinsâ C. W. Evans, V. Gubala, R. Nooney, D. E. Williams, M. A. Brimble and A. L. De Vries, Antarctic Science, 2011, 23, 57-64. http://dx.doi.org/10.1017/S0954102010000635
⢠(Selected to the Faculty of 1000 http://f1000.com/9089956) (IF = 1.6)
245. âSynthesis of Methyl N-Boc-(2S, 4R)-4-Methylpipecolateâ K. Y. Hung, P. W. R. Harris and M. A. Brimble,
Journal of Organic Chemistry, 2010, 75, 8728-8731. (IF = 4.6) https://doi.org/10.1021/jo102038q
244. âSynthesis of a Functionalised 7,6-Bicyclic Spiroimine Ring Fragment of the Spirolidesâ S. M. Gueret, D. P. Furkert and M. A. Brimble, Organic Letters, 2010, 12, 5226-5229. (IF = 5.9) https://doi.org/10.1021/ol102525w
243. âStereoselective Synthesis of 4-Substituted 4-Hydroxypiperidines via Epoxidation-Ring Opening of 4-Methylenepiperidinesâ V. A. McKay, S. J. Thompson, P. M. Tran, K. J. Goodall, M. A. Brimble and D. Barker, Synlett, 2010, 17, 2631-2635. (IF = 2.7) http://dx.doi.org/10.1055/s-0030-1258778
242. âHetero-Directed Reverse Wacker Oxidations. Synthesis of the Reported Structure of (â)-Herbaric Acidâ P. J. Choi, J. Sperry and M. A. Brimble, Journal of Organic Chemistry, 2010, 75, 7388-7392. (IF = 4.6) https://doi.org/10.1021/jo1016585
241. âA Double Mannich Approach to the Synthesis of Substituted Piperidones – Application to the Synthesis of Substituted E-ring Analogues of Methyllycaconitineâ Y. Chan, J. Balle, J. K. Sparrow, P. D. W. Boyd, M. A. Brimble, D. Barker, Tetrahedron, 2010, 66, 7179-7191. (IF = 2.8) https://doi.org/10.1016/j.tet.2010.06.084
240. âGrowth Habit Modification of Ice Crystals using Antifreeze Glycoprotein (AFGP) Analoguesâ R. Peltier, C. W. Evans, A. L. DeVries, M. A. Brimble, A. J. Dingley and D. E. Williams, Crystal Growth and Design, 2010, 10, 5066-5077. (IF = 4.72) https://doi.org/10.1021/cg1005083
239. âSynthesis of the Pyranonaphthoquinones Dehydroherbarin, (+)-Astropaquinone B and (+)-Astropaquinone C en route to Ascomycones A and Bâ A. Wadsworth, J. Sperry and M. A. Brimble, Synthesis, 2010, 2604-2608. (IF = 2.5) http://dx.doi.org/10.1055/s-0029-1218832
238. âSynthesis of the FG Ring Fragment of Pectenotoxins 1-9â A. Heapy and M. A. Brimble, Tetrahedron, 2010, 66, 5424-5431. (IF = 2.8) https://doi.org/10.1016/j.tet.2010.05.027
237. âSynthesis of the Bis-Spiroacetal C25âC40 Moiety of the Antimitotic Agent Spirastrellolide B using a Bis-Dithiane Deprotection/Spiroacetalisation Sequenceâ J. L.-Y. Chen and M. A. Brimble, Chemical Communications, 2010, 46, 3967-3969. (IF = 5.8) https://doi.org/10.1039/C0CC00056F
236. âSynthesis of Triazole Analogues of the Nanaomycin Antibiotics using âClick Chemistryâ â K. Rathwell, J. Sperry and M. A. Brimble, Tetrahedron, 2010, 66, 4002-4009. (IF = 2.8) https://doi.org/10.1016/j.tet.2010.04.048
235. âA Flexible Asymmetric Synthesis of the Tetracyclic Core of Berkelic Acid using a Horner-Wadsworth-Emmons/oxa-Michael Cascadeâ Z. E. Wilson and M. A. Brimble, Organic and Biomolecular Chemistry, 2010, 8, 1284-1286. (IF = 3.7) https://doi.org/10.1039/B927219B
234. âTotal Synthesis and Absolute Configuration of (-)-Berkeleyamide Aâ J. Sperry, E. B. J. Harris and M. A. Brimble, Organic Letters, 2010, 12, 420-423. (IF = 5.3) https://doi.org/10.1021/ol902525k
233. âMetal Binding Studies Using Spiroacetal Crown Ethersâ M. Nikac, M. A. Brimble, R. L. Crumbie and T. D. Bailey, Tetrahedron Letters, 2010, 51, 1072-1074. (IF = 2.7) https://doi.org/10.1016/j.tetlet.2009.12.110
232. âImproved Synthesis of the Benzyne Precursor 2-(Trimethylsilyl)phenyl Trifluoromethanesulfonateâ D. J. Atkinson, J. Sperry and M. A. Brimble, Synthesis, 2010, 911-913. (IF = 2.5) https://doi.org/10.1016/10.1055/s-0029-1218631
231. âMicrowave Assisted Synthesis of Fluorescein-Labelled GalNAcďĄ1-O-Ser/Thr (Tn) Glycopeptides as Immunological Probesâ D. J. Lee, P. W. R. Harris, R. Kowalczyk, P. R. Dunbar and M. A. Brimble, Synthesis, 2010, 763-769. (IF = 2.5) http://dx.doi.org/10.1055/s-0029-1218635
230. âTowards the Total Chemical Synthesis of the Cancer Protein NY-ESO-1â P. W. R. Harris and M. A. Brimble, Biopolymers (Peptide Science), 2010, 94, 542-550. (IF = 2.9) https://doi.org/10.1002/bip.21351
⢠(Invited paper for Special Issue of Peptide Science dedicated to Professor Steve Kent)
229. âA One-pot Approach to Neoglycopeptides using Orthogonal Native Chemical Ligation and Click Chemistryâ D. J. Lee, K. Mandal, P. W. R. Harris, M. A. Brimble and S. B. H. Kent, Organic Letters, 2009, 11, 5270-5273. (IF = 5.4) https://doi.org/10.1021/ol902131n
228. âSynthesis and Reactivity of beta-Methoxymethyl Enecarbamatesâ P. D. OâConnor, M. G. Marino, S. M. Gueret and M. A. Brimble, Journal of Organic Chemistry, 2009, 74, 8893-8896. (IF = 4.805) https://doi.org/10.1021/jo901992z
227. âPyranonaphthoquinone Derivatives of Eleutherin, Ventiloquinone L, Thysanone and Nanaomycin A Possessing a Diverse Topoisomerase II Inhibition and Cytotoxicity Spectrumâ J. Sperry, I. Loreno-Castrillejo, M. A. Brimble and F. Machin, Bioorganic and Medicinal Chemistry, 2009, 17, 7131-7137. https://doi.org/10.1016/j.bmc.2009.08.064
226. âAn Efficient Formal Synthesis of the Human Telomerase Inhibitor (Âą)-Îł-Rubromycinâ D. C. K. Rathwell, S.-H. Yang, K.Y. Tsang and M.A. Brimble, Angewandte Chemie International Edition, 2009, 48, 7996-8000. https://doi.org/10.1002/anie.200903316
⢠(Selected for âfrontispieceâ and as a very important paper (VIP) -only 5% of papers selected as VIP papers)
225. âSynthesis of an Arginine Tagged [Cys155-Arg180] Fragment of NY-ESO-1: Elimination of an Undesired By-product using “In House” Resinsâ P. W. R. Harris and M. A. Brimble, Synthesis, 2009, 3460-3466. https://doi.org/10.1055/s-0029-1216952
224. âA Novel Approach to Monobenzannulated Spiroketals Using Styrene in the Kulinkovich Reactionâ I. Haym and M. A. Brimble, Synlett, 2009, 2315-2319. https://doi.org/10.1055/s-0029-1217708
223. âSynthesis of (+)-Wine Lactone and its Analogues by a Diels-Alder Approachâ P. D. OâConnor, U. B. Kim and M. A. Brimble, European Journal of Organic Chemistry, 2009, 26, 4405-4411. https://doi.org/10.1002/ejoc.200900486
⢠(Selected for âfront coverâ)
222. âSynthesis of Fish Antifreeze Neoglycopeptides Using Microwave-Assisted âClick Chemistryâ N. Miller, G. M. Williams and M. A. Brimble, Organic Letters, 2009, 11, 2409-2412. https://doi.org/10.1021/ol9005536
221. âBiomimetic Studies Towards the Cardinalins: Synthesis of (+)-Ventiloquinone L and an Unusual Dimerisationâ J. Sperry, J. J. P. Sejberg, F. M. Stiemke and M. A. Brimble, Organic and Biomolecular Chemistry, 2009, 7, 2599-2603. https://doi.org/10.1039/B905077A
220. âEnantioselective Synthesis of the 3C-Protease Inhibitor (â)-Thysanone using a Staunton-Weinreb Annulation Strategyâ J. Sperry, T. Y. Yuen and M. A. Brimble, Synthesis, 2009, 2561-2569. https://doi.org/10.1055/s-0029-1217390
219. âInfluence of alpha-Methyl Substitution of Proline-based Organocatalysts on the Asymmetric alpha-Oxidation of Aldehydesâ S. -T. Tong, M. A. Brimble and D. Barker, Tetrahedron, 2009, 65, 4801-4807. https://doi.org/10.1016/j.tet.2009.04.060
218. âStability of 5(6)-Carboxyfluorescein in Microwave Assisted Synthesis of Fluorescein-Labelled O-Dimannosylated Peptidesâ R. Kowalczyk, P. W. R. Harris, R. P. Dunbar and M. A. Brimble, Synthesis, 2009, 2210-2222. http://dx.doi.org/10.1055/s-0029-1216820
217. âSynthetic Studies Towards the Anti-inflammatory Agent, Oleocanthal using a JohnsonâClaisen (orthoester) Rearrangement Strategy,â J. -T. B. Kueh, P. D. OâConnor, H. HĂźgel and M. A. Brimble, Archive for Organic Chemistry (ARKIVOC), 2009, (vii), 58-71. http://dx.doi.org/10.3998/ark.5550190.0010.706
216. âUse of Click Chemistry for the Synthesis of Tetrazole-Containing Analogues of the Neuroprotective Agent Glycyl-L-prolyl-L-glutamic Acid (GPE)â K.-Y. Hung, P. W. R. Harris and M. A. Brimble, Synlett, 2009, 1233-1236. http://dx.doi.org/10.1055/s-0028-1088128
215. âSynthesis of AE and BE Ring Analogues of the Alkaloid Methyllycaconitineâ H. Guthmann, D. Conole, E. Wright, K. Koerber, D. Barker and M. A. Brimble, European Journal of Organic Chemistry, 2009, 1944-1960. https://doi.org/10.1002/ejoc.200900030
214. âSynthesis of 6,6-Bisbenzannulated Spiroketals Related to the Rubromycins Using a Double Intramolecular Hetero-Michael Addition (DIHMA)â P. Choi, D. C. K. Rathwell and M. A. Brimble, Tetrahedron Letters, 2009, 50, 3245-3248. https://doi.org/10.1016/j.tetlet.2009.02.030
⢠(Invited Article for the special edition to mark the 50th Golden Anniversary of Tetrahedron Letters).
213. âA Facile Cross Metathesis-Radical Cyclisation Approach to Monobenzannulated Spiroketalsâ Y.-C. Liu, J. Sperry, D. C. K. Rathwell and M. A. Brimble, Synlett, 2009, 793-797. https://doi.org/10.1055/s-0028-1087942
212. âSynthesis of Enantiopure Bicyclic alpha,alpha-Disubstituted Spirolactams via Asymmetric Birch Reductive Alkylationâ S. M. GuĂŠret, P. D. OâConnor and M. A. Brimble, Organic Letters, 2009, 11, 963-966. https://doi.org/10.1021/ol8029017
211. âSynthesis of Spiroacetal-Nucleosides as Privileged Natural Product-like Scaffoldsâ K. W. Choi and M. A. Brimble, Organic and Biomolecular Chemistry, 2009, 7, 1424-1436. https://doi.org/10.1039/B818314G
210. âA Novel Approach to the CDE Ring System of Pectenotoxin-4 Triggered by VO(acac)2 Induced Epoxy-Acetalizationâ S. Carley and M. A. Brimble, Organic Letters, 2009, 11, 563-566. https://doi.org/10.1021/ol8025457
209. âIn vitro Metabolism of Norbormide in Rat, Mouse and Guinea Pig Liver Preparationsâ S. Ravindran, B. Hopkins, S. Bova, D. Rennison, M. A. Brimble and M. Tingle, Environmental Toxicology and Pharmacology, 2009, 27, 144-148. https://doi.org/10.1016/j.etap.2008.09.007
208. âNNZ-2566: A GlyâProâGlu Analogue With Neuroprotective Efficacy in a Rat Model of Acute Focal Strokeâ M. J. Bickerdike, G. B. Thomas, D. C. Batchelor, E. S. Sirmianne, W. Leong, H. Lai, F. Sieg, J. Wen, M. A. Brimble, P. W. R. Harris and P. D. Gluckman, Journal of the Neurological Sciences, 2009, 278, 85-90. https://doi.org/10.1016/j.jns.2008.12.003
207. â3-Allyl-2-hydroxy-5,6,8-trimethoxynaphthalene-1,4-dioneâ D. C. Rathwell, K. Y. Tsang, K. W. Choi, P. D. W. Boyd, and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2008, E64, O1929. https://dx.doi.org/10.1107%2FS1600536808028432
206. âEnantioselective Synthesis of the Dimeric Pyranonaphthoquinone Core of the Cardinalins Using a Late-Stage Homocoupling Strategyâ J. Sperry, J. S. Gibson, J. J. P. Sejberg and M. A. Brimble, Organic and Biomolecular Chemistry, 2008, 6, 4261-4270. https://doi.org/10.1039/B813605J
205. “Diastereoselective Synthesis of Substituted 4-Piperidones and 4-Piperidols Using a Double Mannich Reaction” Y. Chan, H. Guthmann, M. A. Brimble and D. Barker, Synlett, 2008, 2601-2604. https://doi.org/10.1055/s-0028-1083522
204. “The Synthesis of Phosphopeptides Using Microwave-assisted Solid Phase Peptide Synthesis” P. W. R. Harris, G. M. Williams, P. Shepherd and M. A. Brimble, International Journal of Peptide Research and Therapeutics, 2008, 14, 387-392. https://doi.org/10.1007/s10989-008-9149-9
203. âracemic-N-(3-hydroxy-1,2-diphenylpropyl)-4-methylbenzenesulfonamideâ S. T. Tong, D. Barker, K. W. Choi, P. D. W. Boyd and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2008, E64, O1990. https://dx.doi.org/10.1107%2FS1600536808028948
202. âracemic-2′-Phenylcyclohexanespiro-4′-(azepano[1,2-b]isoxazolidine)â D. Crimmins, K. W. Choi, P. D. W. Boyd, and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2008, E64, O1535. http://dx.doi.org/10.1107/S1600536808021867
201. âA Facile Synthesis of a Spironitrone and a Study of its Cycloaddition and Nucleophilic Addition Reactionsâ D. Crimmins, I. Dimitrov, P. D. OâConnor, V. Caprio and M. A. Brimble, Synthesis, 2008, 3319-3325. http://dx.doi.org/10.1055/s-0028-1083151
200. âSynthesis of Spiroacetal-Triazoles as Privileged Natural Product-Like Scaffolds Using âClick Chemistryââ K. W. Choi and M. A. Brimble, Organic and Biomolecular Chemistry, 2008, 6, 3518-3526. https://doi.org/10.1039/B808454H
⢠(Invited paper for special issue to honour Professor Andrew Holmesâs 65th birthday, selected for âfront coverâ)
199. âAn Efficient Enantioselective Synthesis of the 3C Protease Inhibitor (â)-Thysanoneâ J. Sperry and M. A. Brimble, Synlett, 2008, 1910-1912. http://dx.doi.org/10.1055/s-2008-1078590
198. â(1R,6R)-1-Methyl-8-azaspiro[5.6]dodecan-7-oneâ S. M. GuĂŠret, K. W. Choi, P. D. O’Connor, P. D. W. Boyd and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2008, E64, O1151. http://dx.doi.org/10.1107/S1600536808015158
197. âBuchwald-Hartwig Mono-N-arylation of 2,6-Dihaloisonicotinic Acid Derivatives: A Convenient Desymmetrization Methodâ A. V. Lorimer, P. D. OâConnor and M. A. Brimble, Synthesis, 2008, 2764-2770. http://dx.doi.org/10.1055/s-2008-1067208
196. âanti-Helicobacter pylori Activity of Derivatives of the Phthalide-Containing Antibacterial Agents Spirolaxane Methyl Ether, CJ-12,954, CJ-13,013, CJ-13,102, CJ-13,104, CJ-13,108 and CJ-13,015â F. J. Radcliff, J. D. Fraser, Z. E. Wilson, A. M. Heapy, J. E. Robinson, C. J. Bryant, C. L. Flowers and M. A. Brimble, Bioorganic and Medicinal Chemistry, 2008, 16, 6179-6185. https://doi.org/10.1016/j.bmc.2008.04.037
195. â(1R,1´R,3S,3´S)-5,5´,10,10´-Tetramethoxy-1,1´,3,3´-tetramethyl-3,3´,4,4´-terahydro-1H,1´H-8,8´-bibenzo[g]isochromeneâ J. J. P. Sejberg, J., Sperry, K. W. Choi, P. D. W. Boyd and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2008, E64, O758. https://doi.org/10.1107/s1600536808007599
194. âracemic-1-{8´-(tert-Butyldiphenylsilyloxymethyl)-1´,7´-dioxaspiro[5.5]undecan-2´-yl}uridineâ K. W. Choi, M. A. Brimble and T. Groutso, Acta Crystallographica, Section E: Structure Reports Online, 2008, E64, O715. https://dx.doi.org/10.1107%2FS1600536808006727
193. âNovel Use of N-Carboalkoxy alpha,beta-Unsaturated Iminium Ions as Dienophiles in Diels-Alder Reactionsâ P. D. OâConnor, K. Koerber and M. A. Brimble, Synlett, 2008, 1036-1038. http://dx.doi.org/10.1055/s-2008-1072658
192. âA Facile Enantioselective Synthesis of the Dimeric Pyranonaphthoquinone Core of the Cardinalinsâ M. A. Brimble, J. S. Gibson, J. J. P. Sejberg and J. Sperry, Synlett, 2008, 867-870. http://dx.doi.org/10.1055/s-2008-1042896
191. â1H and 13C NMR Spectra for C-6 and C-9 Substituted 3-Azabicyclo[3.3.1]nonanesâ K. J. Goodall, M. A. Brimble and D. Barker, Magnetic Resonance in Chemistry, 2008, 46, 75-79. http://dx.doi.org/10.1002/mrc.2100
190. âAn Approach to an Enantioselective Synthesis of Crisamicin A via a Novel Double Hauser-Kraus Annulation Strategyâ O. Andrey, J. Sperry, U. S. Larsen and M. A. Brimble, Tetrahedron, 2008, 64, 3912-3927. https://doi.org/10.1016/j.tet.2008.02.065
189. âSynthesis of a C8 Oxygenated Pyranonaphthoquinone: A Useful Precursor to Dimeric Pyranonaphthoquinonesâ P. Bachu, M. A. Brimble and J. Sperry, Tetrahedron, 2008, 64, 3343-3350. https://doi.org/10.1016/j.tet.2008.01.135
188. âChemoenzymatic Synthesis of Deoxy Analogues of the DNA Topoisomerase II Inhibitor Eleutherin and the 3C-Protease Inhibitor Thysanoneâ P. Bachu, J. Sperry and M. A. Brimble, Tetrahedron, 2008, 64, 4827-4834. https://doi.org/10.1016/j.tet.2008.01.112
⢠(Invited Article for Tetrahedron Symposia-in-Print â âNatural Products Synthesisâ)
187. âSynthesis of Fluorescein-Labelled O-Mannosylated Peptides as Components for Synthetic Vaccines: Comparison of Two Synthetic Strategiesâ M. A. Brimble, R. Kowalczyk, P. W. R. Harris, P. R. Dunbar and V. J. Muir, Organic and Biomolecular Chemistry, 2008 6, 112-121. https://doi.org/10.1039/b712926b
186. âUse of (S)-5-(2-Methylpyrrolidin-2-yl)-1H-tetrazole as a Novel and Enantioselective Organocatalyst for the Aldol Reactionâ S.-T. Tong, P. W. R. Harris, D. Barker and M. A. Brimble, European Journal of Organic Chemistry, 2008, 164-170. https://doi.org/10.1002/ejoc.200700834
⢠(One of the most often downloaded articles in Wiley InterScience).
185. âracemic-Cyclohexane-1,2-diyl Bis(4-nitrobenzoate)â S. T. Tong, D. Barker, K. W. Choi, P. D. W. Boyd and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2008, E64, O2174. https://dx.doi.org/10.1107%2FS1600536808033874
184. âA Comparative Study of the Different Glycosylation Methods for the Synthesis of D-Mannopyranosides of N-alpha-fluorenylmethoxycarbonyl-trans-4-hydroxy-L-proline Allyl Esterâ D. J. Lee, R. Kowalczyk, V. J. Muir, P. M. Rendle and M. A. Brimble, Carbohydrate Research, 2007, 342, 2628-2634. https://doi.org/10.1016/j.carres.2007.08.015
183. âPeripheral Administration of a Novel Diketopiperazine, NNZ 2591, Prevents Brain Injury and Improves Somatosensory-Motor Function Following Hypoxia-ischemia in Adult Ratsâ J. Guan, S. Matai, P. W .R. Harris, M. A. Brimble, J.-Y. Wen, R. Zhang and P. D. Gluckman, Neuropharmacology, 2007, 53, 749-762. https://doi.org/10.1016/j.neuropharm.2007.08.010
182. âSynthesis of Mannosylated Glycopeptides as Components for Synthetic Vaccinesâ R. Kowalczyk, M. A. Brimble and R. Dunbar, Peptide Science 2007, 88, 539 and in âAdvances in Experimental Medicine and Biology,â 2009, 611, 351-352. https://doi.org/10.1007/978-0-387-73657-0_155
181. âSynthesis and Assignment of the Absolute Configuration of the anti-Helicobacter pylori Agents CJ-12,954 and CJ-13,014â M. A. Brimble and C. J. Bryant, Organic and Biomolecular Chemistry, 2007, 5, 2858-2866. https://doi.org/10.1039/b709932k
180. âSynthesis of the FG Fragment of the Pectenotoxinsâ A. M. Heapy, T. W. Wagner and M. A. Brimble, Synlett, 2007, 2359-2362. http://dx.doi.org/10.1055/s-2007-985600
179. âThe Influence of Microwave Irradiation on Lipase-Catalyzed Kinetic Resolution of Racemic Secondary Alcoholsâ P. Bachu, J. S. Gibson, J. Sperry and M. A. Brimble, Tetrahedron Asymmetry, 2007, 18, 1618-1624. https://doi.org/10.1016/j.tetasy.2007.06.035
178. âSynthesis of the anti-Helicobacter pylori Agent (+)-Spirolaxine Methyl Ether and the Unnatural (2âS)-Diastereomerâ J. Robinson and M. A. Brimble, Organic and Biomolecular Chemistry, 2007, 5, 2572-2582. https://doi.org/10.1039/B708265G
177. âEnantioselective Synthesis of an Analogue of Nanaomycin Aâ M. A. Brimble, P. Bachu and J. Sperry, Synthesis, 2007, 2887-2893. http://dx.doi.org/10.1055/s-2007-983848
176. âA Short Enantioselective Synthesis of the Topoisomerase II Inhibitor (+)-Eleutherinâ J. S. Gibson, O. Andrey and M. A. Brimble, Synthesis, 2007, 2611-2613. http://dx.doi.org/10.1055/s-2007-983841
175. â1H and 13C NMR Spectra of Methylmaleimido- and Methylsuccinimidoanthranilate Esters of 1-Hydroxymethyl-6-methoxy-3-azabicyclo[3.3.1]nonanesâ K. J. Goodall, M. A. Brimble and D. Barker, Magnetic Resonance in Chemistry, 2007, 45, 695-699. https://doi.org/10.1002/mrc.2027
174. âAssessing the Molecular Basis for Rat-Selective Induction of the Mitochondrial Permeability Transition by Norbormideâ A. Zulian, V. Petronilli, S. Bova, F. Dabbeni-Sala, G. Cargnelli, M. Cavalli, D. Rennison, J. Stäb, O. Laita, D. J. Lee, M. A. Brimble, B. Hopkins, P. Bernardi and F. Ricchelli, Biochimica et Biophysica Acta, Bioenergetics, 2007, 1767, 980-988. https://doi.org/10.1016/j.bbabio.2007.04.002
173. âSynthesis of Aromatic Spiroacetals Related to gamma-Rubromycin Based on a 3H-Spiro[1-benzofuran-2,2â-chromane] Skeletonâ K. Y. Tsang and M. A. Brimble, Tetrahedron, 2007, 63, 6015-6034. http://dx.doi.org/10.1016/j.tet.2007.02.033
⢠(Invited Paper for Special 50th Anniversary Issue of Tetrahedron)
172. âSynthesis of Indole Analogues of the anti-Helicobacter pylori Compounds CJ-13,015, CJ-13,102, CJ-13,104 and CJ-13,108â Z. E. Wilson, A. M. Heapy and M. A. Brimble, Tetrahedron, 2007, 63, 5379-5385. https://doi.org/10.1016/j.tet.2007.04.067
171. âA Facile Synthesis of Aryl Spirodioxines Based on a 3H,3âH-2,2â-Spirobi(benzo[b][1,4]dioxane) Skeletonâ M. A. Brimble, Y.-C. Liu and M. Trzoss, Synthesis, 2007, 1392-1402. http://dx.doi.org/10.1055/s-2007-966016
170. âSynthesis and Activity Studies of Analogues of the Rat Selective Toxicant Norbormideâ D. Rennison, S. Bova, M. Cavalli, F. Ricchelli, A. Zulian, B. Hopkins and M. A. Brimble, Bioorganic and Medicinal Chemistry, 2007, 15, 2963-2974. https://doi.org/10.1016/j.bmc.2007.02.012
169. âSynthesis of Thiacrown and Azacrown Ethers Based on a Spiroacetal Frameworkâ M. A. Brimble, M. Nikac and R. Crumbie, Tetrahedron, 2007, 63, 5220-5226. https://doi.org/10.1016/j.tet.2007.03.174
168. âSynthesis of Isotopically Labelled Thiol Volatiles and Cysteine Conjugates for Quantification of Sauvignon Blanc Wineâ K. R. Hebditch, L. Nicolau and M. A. Brimble, Journal of Labelled Compounds and Radiopharmaceuticals, 2007, 50, 237-243. https://doi.org/10.1002/jlcr.1262
167. âSynthesis of a C-Terminal Thioester Derivative of the Lipopeptide Pam2CSKKKKG Using Fmoc SPPSâ P. W. R. Harris, M. A. Brimble, R. Dunbar and S. B. H. Kent, Synlett, 2007, 713-716. http://dx.doi.org/10.1055/s-2007-970759
166. âA Facile Synthesis of 1,1â-Spirobi(3H,3âH)isobenzofuransâ M. A. Brimble and C. V. Burgess, Synthesis, 2007, 754-760. http://dx.doi.org/10.1055/s-2007-965911
165. âSynthesis of a Regioisomeric Analogue of the 3C-Protease Inhibitor Thysanone via a Hauser Annulation Strategyâ M. A. Brimble, S. I. Houghton and P. D. Woodgate, Tetrahedron, 2007, 63, 880-887. https://doi.org/10.1016/j.tet.2006.11.046
164. âSynthesis of the Spiroacetal-Containing anti-Helicobacter pylori Agents CJ-12,954 and CJ-13,014â
M. A. Brimble and C. J. Bryant, Chemical Communications, 2006, 4506-4508. https://doi.org/10.1039/b612757f
163. âSynthesis of New Aza-C-disaccharides Linking 4-Deoxy-4-amino-beta-L-erythro-furanose to C-2 of D-Glucose and D-Alloseâ E. RodrĂguez Garcia, M. A. Brimble and P. Vogel, European Journal of Organic Chemistry, 2006, 3845-3855. https://doi.org/10.1002/ejoc.200600199
162. â1H and 13C NMR Data for C-6 Substituted 3-Azabicyclo[3.3.1]nonane-1-carboxylatesâ K. Goodall, M. A. Brimble and D. Barker, Magnetic Resonance in Chemistry, 2006, 44, 980-983. https://doi.org/10.1002/mrc.1878
161. âSynthesis of Macrocyclic Analogues of the Neuroprotective Agent Glycyl-L-prolyl-L-glutamic Acid (GPE)â
P. W. R. Harris and M. A. Brimble, Organic and Biomolecular Chemistry, 2006, 4, 2696-2709. https://doi.org/10.1039/b605293b
160. âSynthesis of N-(3-Phenylpropyl)-substituted Tricyclic ABE Ring Analogues of the Alkaloid Methyllycaconitineâ A. Lehmann, C. Brocke, D. Barker and M. A. Brimble, European Journal of Organic Chemistry, 2006, 3205-3215. http://dx.doi.org/10.1002/ejoc.200600326
159. âSynthesis of the Bis-Spiroacetal Moiety of the Shellfish Toxins Spirolides B and D Using an Iterative Oxidative Radical Cyclization Strategyâ K. Meilert and M. A. Brimble, Organic and Biomolecular Chemistry, 2006, 4, 2184-2192. https://doi.org/10.1039/b604334h
⢠(Hot article and selected for âfront coverâ).
158. âA Novel Bromine-Induced Ring Expansion of the Spiroimine Moiety of the Shellfish Toxin Gymnodimineâ M. A. Brimble, J. E. Robinson, J. Merten, V. Beuzenberg, M. Dragunow, P. Holland and D. Mountfort, Synlett, 2006, 1610-1612. http://dx.doi.org/10.1055/s-2006-941605
157. âSynthesis of Isotopically Labelled Glycyl-L-prolyl-L-glutamic Acid (GlypromateÂŽ) and Derivativesâ P. W. R. Harris and M. A. Brimble, Journal of Labelled Compounds and Radiopharmaceuticals, 2006, 49, 571-581. https://doi.org/10.1002/jlcr.1075
156. âA Facile Synthesis of Fused Aromatic Spiroacetals Based on the 3,4,3â,4â-Tetrahydro-2,2â-spirobis(2H-1-benzopyran) Skeletonâ M. A. Brimble, C. Flowers, M. Trzoss and K. Y. Tsang, Tetrahedron, 2006, 62, 5883-5896. http://dx.doi.org/10.1016/j.tet.2006.04.026
155. â(2”S,5”R,7”S)-2-[2′-(2”-Methyl-1”,6”-dioxaspiro-[4.5]dec-7”-yl)ethylsulfonyl]-1,3-benzothiazoleâ G. R. Clark, J. E. Robinson and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2006, E62, O1187-O1188. http://dx.doi.org/10.1107/S1600536806006544
154. âSynthesis of the ABC Tricyclic Fragment of the Pectenotoxins via Stereocontrolled Cyclization of a gamma-Hydroxyepoxide Appended to the AB Spiroacetal Unitâ R. Halim, M. A. Brimble and J. Merten, Organic and Biomolecular Chemistry, 2006, 4, 1387-1399. https://doi.org/10.1039/B600951D
153. â8′-Methoxy-3H-spiro[1-naphthofuran-2,2′-chromane]â G. R. Clark, K. Y. Tsang and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2006, E62, O1075-O1076. http://dx.doi.org/10.1107/S1600536806005125
152. âAddition of 2-tert-Butyldimethylsilyloxythiophene to Activated Quinones: An Approach to Thia Analogues of Kalafunginâ M. A. Brimble, O. S. Laita and J. E. Robinson, Tetrahedron, 2006, 62, 3021-3027. https://doi.org/10.1016/j.tet.2006.01.040
151. âSynthesis of the Phthalide-Containing anti-Helicobacter pylori agents CJ-13,015, CJ-13,102, CJ-13,103, CJ-13,104 and CJ-13,108â M. A. Brimble, C. L. Flowers, J. K. Hutchinson, J. E. Robinson and M. Sidford, Tetrahedron, 2005, 61, 10036-10047. https://doi.org/10.1016/j.tet.2005.08.027
150. âSynthesis of Proline-Modified Analogues of the Neuroprotective Agent Glycyl-L-prolyl-glutamic Acid (GPE)â P. W. R. Harris, M. A. Brimble, V. J. Muir, M. Y. H. Lai, N. S. Trotter and D. J. Callis, Tetrahedron, 2005, 61, 10018-10035. https://doi.org/10.1016/j.tet.2005.08.026
149. âSynthesis of the Bis-Spiroacetal Moiety of Spirolides B and Dâ K. Meilert and M. A. Brimble, Organic Letters, 2005, 7, 3497-3500. https://doi.org/10.1021/ol051260u
148. â5,8′-Dimethoxy-3H-1-benzofuran-2-spiro-2′-chromanâ G. R. Clark, K. Y. Tsang and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2005, E61, O2748-O2749. https://doi.org/10.1107/S1600536805023731
147. â5-Methoxyspiro[1-benzofuran-2(3H),2′-chroman]â G. R. Clark, K. Y. Tsang and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2005, E61, O1123-O1124. https://doi.org/10.1107/S1600536805008743
146. â6,8′-Dimethoxy-2,2′-spirobichromanâ G. R. Clark, C. L. Flowers and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2005, E61, O910-O911. https://doi.org/10.1107/S1600536805006938
145. âSynthesis of the ABC Fragment of the Pectenotoxinsâ R. Halim, M. A. Brimble and J. Merten, Organic Letters, 2005, 7, 2659-2662. https://doi.org/10.1021/ol0507975
144. âMethyllycaconitine Analogues have Mixed Antagonist Effects at Nicotinic Acetylcholine Receptorsâ
D. Barker, D. H.-S. Lin, J. E. Carland, C. P.-Y Chu, M. Chebib, M. A. Brimble, G. P. Savage and M. D. McLeod, Bioorganic and Medicinal Chemistry, 2005, 13, 4565-4575. https://doi.org/10.1016/j.bmc.2005.04.054
143. âUse of Bis(aminol) Ethers derived from N-(S)-(â)-alpha-Methylbenzylamine in Reactions With Resorcinarenes and Double Mannich Reactionsâ B. R. Buckley, P. C. Bulman-Page, H. Heaney, E. P Sampler, S. Carley, C. Brocke and M. A. Brimble, Tetrahedron, 2005, 61, 5876-5888. https://doi.org/10.1016/j.tet.2005.03.130
142. âInvestigations into the Cellular Actions of the Shellfish Toxin Gymnodimine and Analoguesâ M. Dragunow, M. Trzoss, M. A. Brimble, R. Cameron, V. Beuzenberg, P. Holland and D. Mountfort, Environmental Toxicology and Pharmacology, 2005, 20, 305-312. https://doi.org/10.1016/j.etap.2005.02.008
141. âEfficient Synthesis of the Azabicyclo[3.3.1]nonane Ring System in the Alkaloid Methyllycaconitine Using Bis(alkoxymethyl)alkylamines as Aminoalkylating Agents in a Double Mannich Reactionâ M. A. Brimble and C. Brocke, European Journal of Organic Chemistry, 2005, 2385-2396. https://doi.org/10.1002/ejoc.200500003
140. âThe First Enantioselective Total Synthesis of the anti-Helicobacter pylori Agent (+)-Spirolaxine Methyl Etherâ J. Robinson and M. A. Brimble, Chemical Communications, 2005, 1560-1562. https://doi.org/10.1039/B418106A
139. â(1S,2S)-1-{2-[(4-Methoxybenzyl)oxy]ethyl}-2-methyl-3-butenyl (1S,4R)-4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylateâ K. T. Meilert, G. R. Clark, T. Groutso and M. A. Brimble, Acta Crystallographica, Section E: Structure Reports Online, 2005, E61, O6-O7. http://dx.doi.org/10.1107/S1600536804030946
138. âSynthesis of Spirolactams via Diels-Alder Addition of 1,3-Butadienes to alpha-Methylenelactamsâ D. Crimmins, M. Trzoss and M. A. Brimble, Archive for Organic Chemistry (ARKIVOC), 2005, (i), 39-52. http://dx.doi.org/10.3998/ark.5550190.0006.105
137. âSynthesis and Pharmacological Evaluation of Side Chain Modified Glutamic Acid Analogues of the Neuroprotective Agent Glycyl-L-prolyl-L-glutamic Acid (GPE)â M. A. Brimble, N. S., Trotter, P. W. R. Harris, M. S. Levi and F. Sieg, Bioorganic and Medicinal Chemistry, 2005, 13, 519-532. https://doi.org/10.1016/j.bmc.2004.10.006
136. âSynthesis and Neuroprotective Activity of Analogues of Glycyl-L-prolyl-L-glutamic Acid (GPE) Modified at the alpha-Carboxylic Acidâ N. S. Trotter, M. A. Brimble, P. W. R. Harris, D. J. Callis and F. Sieg, Bioorganic and Medicinal Chemistry, 2005, 13, 501-517. https://doi.org/10.1016/j.bmc.2004.10.005
135. âSynthesis and Pharmacological Evaluation of Glycine-Modified Analogues of the Neuroprotective Agent Glycyl-L-prolyl-L-glutamic Acid (GPE)â M. Y. H. Lai, M. A. Brimble, D. J. Callis, P. W. R. Harris, M. S. Levi and F. Sieg, Bioorganic and Medicinal Chemistry, 2005, 13, 533-548. https://doi.org/10.1016/j.bmc.2004.10.004
134. âSynthesis of the 1,6,8-Trioxadispiro[4.1.5.2]tetradec-11-ene Ring System Present in the Spirolide Family of Shellfish Toxins and its Conversion into a 1,6,8-Trioxadispiro[4.1.5.2]-tetradec-9-en-12-ol via Base-Induced Rearrangement of an Epoxideâ M. A. Brimble and D. Furkert, Organic and Biomolecular Chemistry, 2004, 2, 3573-3583. https://doi.org/10.1039/b412883d
133. âApplication of a Double Mannich Reaction Using Bis(aminol) Ethers in the Synthesis of AE Ring Analogues of Methyllycaconitineâ C. Brocke, M. A. Brimble, D. S. H. Lin and M. D. McLeod, Synlett, 2004, 2359-2363. http://dx.doi.org/10.1055/s-2004-831340
132. âSynthesis of Simple Analogues of Methyllycaconitine â An Efficient Method for the Preparation of the N-Substituted Anthranilate Pharmacophoreâ D. Barker, M. A. Brimble and M. D. McLeod, Tetrahedron, 2004, 60, 5953-5963. https://doi.org/10.1016/j.tet.2004.05.024
131. âSynthesis of Pyrrolo[3,2-b]benzofurans and Pyrrolo[3,2-b]naphthofurans via Addition of a Silyloxypyrrole to Activated Quinonesâ M. A. Brimble, C. Burgess, R. Halim, M. Petersson and J. Ray, Tetrahedron, 2004, 60, 5751-5758. https://doi.org/10.1016/j.tet.2004.05.008
130. âSynthesis of a Novel Nucleoside Based on a Spiroacetal Frameworkâ M. A. Brimble, J. E. Robinson, K. W. Choi and P. D. Woodgate, Australian Journal of Chemistry, 2004, 57, 665-668. http://dx.doi.org/10.1071/CH04021
129. âSynthesis of Tricyclic Analogues of Methyllycaconitine Using Ring Closing Metathesis to Append a B Ring to an AE Azabicyclic Fragmentâ D. Barker, M. A. Brimble, M. D. McLeod and G. P. Savage, Organic and Biomolecular Chemistry, 2004, 2, 1659-1669. http://dx.doi.org/10.1039/b401119h
128. âA Double Alkylation â Ring Closing Metathesis Approach to Spiroiminesâ M. A. Brimble and M. Trzoss, Tetrahedron, 2004, 60, 5613-5622. https://doi.org/10.1016/j.tet.2004.04.059
127. âTwo Stereoisomers of the Rat Toxicant Norbormideâ P. J. Steel, M. A. Brimble, B. Hopkins and D. Rennison, Acta Crystallographica, Section C: Crystal Structure Communications, 2004, 60, O374-O376. https://doi.org/10.1107/s0108270104006845
126. âSynthesis and Evaluation of Vasoconstrictor and Vasorelaxant Activity of Norbormide Isomersâ M. A. Brimble, V. J. Muir, B. Hopkins and S. Bova, Archive for Organic Chemistry (ARKIVOC), 2004, (i), 1-11.
125. âRadical Oxidative Cyclization of Spiroacetals to Bis-Spiroacetals: An Overviewâ M. A. Brimble, Molecules, 2004, 9, 394-404. http://dx.doi.org/10.3998/ark.5550190.0005.101
124. âUse of a Sonogashira-Acetylide Coupling Strategy for the Synthesis of the Aromatic Spiroketal Skeleton of gamma-Rubromycinâ M. A. Brimble, K. Y. Tsang and J. B. Bremner, Organic Letters, 2003, 5, 4425-4427. https://doi.org/10.1021/ol035723c
123. âSynthesis of Regioisomeric Analogues of Crisamicin Aâ M. A. Brimble and M. Y. H. Lai, Organic and Biomolecular Chemistry, 2003, 1, 4227-4234. https://doi.org/10.1039/B309722F
122. âSynthesis of Spirocyclic Imines: Key Pharmacophores in the Shellfish Toxins Spirolides and Gymnodimineâ M. A. Brimble and M. Trzoss, Synlett, 2003, 2042-2046. http://dx.doi.org/10.1055/s-2003-41481
121. âSynthesis of the Spiroacetal Fragment of Broussonetine Hâ M. A. Brimble, J. H. Park and C. M. Taylor,
Tetrahedron, 2003, 59, 5861-5868. https://doi.org/10.1016/S0040-4020(03)00949-9
120. âSynthesis of Cyclic Proline-Containing Peptides via RingâClosing Metathesisâ M. A. Brimble, P. W. R. Harris and P. D. Gluckman, Organic Letters, 2003, 5, 1847-1850. https://doi.org/10.1021/ol034370e
119. âSuzuki-Miyaura Homocoupling of Naphthyl Triflates Using Bis(pinacolato)diboron: Approaches to the Biaryl Skeleton of Crisamicin Aâ M. A. Brimble and M. Y. H. Lai, Organic and Biomolecular Chemistry, 2003, 1, 2084-2095. https://doi.org/10.1039/B303070A
118. âSynthesis of 3-Azido-2,3,6-trideoxy-beta-D-arabino-hexopyranosyl Pyranonaphthoquinone Analogues of Medermycinâ M. A. Brimble, R. M. Davey, M. D. McLeod and M. Murphy, Organic and Biomolecular Chemistry, 2003, 1, 1690-1700. https://doi.org/10.1039/B301449P
117. âC-Glycosylation of Oxygenated Naphthols with 3-Dimethylamino-2,3,6-trideoxy-L-arabino-hexopyranose and 3-Azido-2,3,6-trideoxy-D-arabino-hexopyranoseâ M. A. Brimble, R. M. Davey, M. D. McLeod and M. Murphy, Australian Journal of Chemistry, 2003, 56, 787-794. http://dx.doi.org/10.1071/CH02236
116. âAddition of 2-[(Trimethylsilyloxy)]furan to 2-Acetyl-1,4-benzoquinone Using Chiral Non-Racemic Copper(II)-pybox Catalystsâ M. A. Brimble, M. D. K. N. Towers and P. D. Woodgate, Archive for Organic Chemistry (ARKIVOC), 2003, (i), 43-55. http://dx.doi.org/10.3998/ark.5550190.0004.106
115. âAddition of Silyloxydienes to 2,6-Dibromo-1,4-benzoquinone: an Approach to Highly Oxygenated Bromonaphthoquinones for the Synthesis of Thysanoneâ D. Barker, M. A. Brimble, P. Do and P. Turner, Tetrahedron, 2003, 59, 2441-2449. https://doi.org/10.1016/S0040-4020(03)00291-6
114. âA Convenient Synthesis of 2-(3-Methyl-2,5-dioxopyrrolidin-1-yl)benzoic Acidâ D. Barker, M. A. Brimble and M. D. McLeod, Synthesis, 2003, 656-658. https://doi.org/10.1055/s-2003-38065
113. âSynthesis of the C10-C22 Bis-Spiroacetal Domain of Spirolides B and D via Iterative Radical Cyclisationâ M. A. Brimble and D. P. Furkert, Organic Letters, 2002, 4, 3655-3658. https://doi.org/10.1021/ol026605c
112. âcis-2-(2-Methoxyphenyl)-3-(phenylselenyl)tetrahydropyranâ C. E. F. Rickard, M. A. Brimble, G. S. Pavia and R. J. Stevenson, Acta Crystallographica, Section E: Structure Reports Online, 2002, E58, O933-O934. https://doi.org/10.1107/S1600536802013272
111. âtrans-2-(2-Naphthyl)-3-(phenylselenyl)tetrahydropyranâ C. Rickard, M. A. Brimble, G. S. Pavia and R. J. Stevenson, Acta Crystallographica, Section E: Structure Reports Online, 2002, E58, O931-O932. http://dx.doi.org/10.1107/S1600536802013260
110. âApplication of Olefin Metathesis to the Synthesis of ABE Ring Analogues of Methyllycaconitineâ D. Barker, M. D. McLeod, M. A. Brimble and G. P. Savage, Tetrahedron Letters, 2002, 43, 6019-6022. https://doi.org/10.1016/S0040-4039(02)01214-5
109. âAddition of a Chiral Non-racemic Silyloxypyrrole to an Activated 1,4-Benzoquinoneâ R. Halim, M. A. Brimble and P. D. Woodgate, Archive for Organic Chemistry (ARKIVOC), 2002, (i), 61-70. http://dx.doi.org/10.3998/ark.5550190.0003.110
108. âSynthesis of Azido Analogue of Medermycinâ M. A. Brimble, R. M. Davey and M. D. McLeod, Synlett, 2002, 1318-1322. http://dx.doi.org/10.1055/s-2002-32955
107. âUncatalyzed Addition of N-(tert-Butoxycarbonyl)-2-tert-butyldimethylsilyloxypyrrole to Activated Quinonesâ M. A. Brimble, R. Halim and M. Petersson, Tetrahedron Letters, 2002, 43, 4777-4780. https://doi.org/10.1016/S0040-4039(02)00932-2
106. âSynthesis of ABE Tricyclic Analogues of Methyllycaconitine Using a Wacker Oxidation â Aldol Strategy to append the B Ring to the AE Fragmentâ D. Barker, M. A. Brimble, M. McLeod, G. P. Savage and D. Wong, Journal of the Chemical Society, Perkin Transactions 1, 2002, 924-931. https://doi.org/10.1039/B200073N
105. âA Facile Synthesis of Aryldihydropyrans Using a Sonogashira-Selenoetherification Strategyâ M. A. Brimble, G. S. Pavia and R. J. Stevenson, Tetrahedron Letters, 2002, 43, 1735-1738. http://dx.doi.org/10.1016/S0040-4039(02)00065-5
104. âStereoselective Synthesis of Deoxy Analogues of the 3C Protease Inhibitor Thysanoneâ M. A. Brimble and R. J. R. Elliott, Tetrahedron, 2002, 58, 183-189. https://doi.org/10.1016/S0040-4020(01)01120-6
103. âSynthesis of a Spiroacetal Intermediate for the Synthesis of the anti-Helicobacter pylori agent CJ-12,954â M. A. Brimble, C. J. Funnell, S. Gorsuch and M. D. Sidford, Archive for Organic Chemistry (ARKIVOC), 2001, (i), 74-87. https://doi.org/10.3998/ark.5550190.0002.106
102. âDetermining the Regio- and Typo-Selectivity of Calf Pregastric Lipaseâ C. J. OâConnor, K. Bang, C. M. Taylor and M. A. Brimble, Journal of Molecular Catalysis B: Enzymatic, 2001, 147-157. https://doi.org/10.1016/S1381-1177(01)00052-2
101. âC-Glycosylation of Naphthols Using Glucosyl Donorsâ M. A. Brimble and T. J. Brenstrum, Archive for Organic Chemistry (ARKIVOC), 2001, (vii), 37-48. http://dx.doi.org/10.3998/ark.5550190.0002.704
100. âSynthesis of a 2-Deoxyglucosyl Analogue of Medermycinâ M. A. Brimble and T. J. Brenstrum, Journal of the Chemical Society, Perkin Transactions 1, 2001, 1624-1634.
99. âC-Glycosylation of Tri-O-benzyl-2-deoxy-D-glucose: Synthesis of Naphthyl Substituted 3,6-Dioxabicyclo[3.2.2]nonanesâ M. A. Brimble and T. J. Brenstrum, Journal of the Chemical Society, Perkin Transactions 1, 2001, 1612-1623.
98. âSynthesis of the Novel 1,7,9-Trioxa[4.1.5.2]-tetradecane Ring System Present in the Spirolidesâ M. A. Brimble, V. Caprio and D. P. Furkert, Tetrahedron, 2001, 57, 4023-4034.
97. âSynthesis of Arylspiroketals Related to the Papulacandins via Generation of Phthalide Oxycarbenium Ionsâ M. A. Brimble, V. Caprio, A. D. Johnston and M. D. Sidford, Synthesis, 2001, 855-862.
96. âA High Yielding Synthesis of Anthranilate Esters from Sterically Hindered Alcoholsâ D. Barker, M. A. Brimble, M. D. McLeod and G. P. Savage, Tetrahedron Letters, 2001, 42, 1785-1788.
95. âSynthesis of the Bis-Spiroacetal Moiety of the Polyether Antibiotic CP44,161â M. A. Brimble, P. R. Allen and H. Prabaharan, Journal of the Chemical Society, Perkin Transactions 1, 2001, 379-389.
94. âendo-(1âR,2âR,5âS,7âS,9âS)-2-(9â-Benzyloxy-2â-phenyl-3â,6â-dioxabicyclo[3.3.2]nonan-7â-yl)-7-bromo-5,8-dimethoxynaphthalen-1-yl acetateâ T. J. Brenstrum, M. A. Brimble and P. Turner, Acta Crystallographica, Section E: Structure Reports Online, 2001, E57, O28-O29.
93. âPolyether Antibiotic CP44,161â P. Allen, M. A. Brimble and P. Turner, Acta Crystallographica, Section C: Crystal Structure Communications, 2001, 57, 95-96.
92. âSynthesis of an Oxaspirolactone Intermediate for the Synthesis of Spirolidesâ M. A. Brimble, F. A. Fares and P. Turner, Australian Journal of Chemistry, 2000, 53, 845-851.
91. âEnantioselective Synthesis of a Cyclopentannulated Kalafungin Analogueâ M. A. Brimble and J. F. McEwan, Archive for Organic Chemistry (ARKIVOC), 2000, (i), 909-916.
90. âDiels-Alder Addition of Acyclic Dienes to Chiral Naphthoquinonesâ M. A. Brimble, R. J. Elliott and J. F. McEwan, Australian Journal of Chemistry, 2000, 53, 571-576.
89. âRegioselective Asymmetric Aminohydroxylation of Precursors to 2,3,6-Trideoxy-3-aminohexosesâ M. A. Brimble, R. M. Davey and M. D. McLeod, Tetrahedron Letters, 2000, 41, 5141-5146.
88. âSynthesis of Aryl Spiroketals Related to the Papulacandins via Allylation of Phthalidesâ M. A. Brimble, V. E. Caprio, A. D. Johnston and M. H. Sidford, Tetrahedron Letters, 2000, 41, 3955-3958.
87. âDiels-Alder Cycloaddition of Cyclopentadiene to a Bis-Naphthoquinoneâ M. A. Brimble and L. J. Duncalf, Molecules, 2000, 5, 162-166.
86. âSynthesis of a C-Glycosylpyranonaphthoquinone Related to Medermycinâ M. A. Brimble and T. J. Brenstrum, Tetrahedron Letters, 2000, 41, 2991-2994.
85. âA Titanium Naphtholate Approach for the Synthesis of Analogues of Griseusin Aâ M. A. Brimble, M. R. Nairn and J. S. O. Park, Journal of the Chemical Society, Perkin Transactions 1, 2000, 697-709.
84. âSynthesis of Naphthyl C-Glycosides of Rearranged Tri-O-benzyl-2-deoxy-D-glucoseâ M. A. Brimble and T. J. Brenstrum, Tetrahedron Letters, 2000, 41, 1107-1110.
83. âReductive Thioalkylation of a Pyranonaphthoquinoneâ M. A. Brimble and M. R. Nairn, Journal of the Chemical Society, Perkin Transactions 1, 2000, 317-322.
82. âReaction of Bromonaphthofurans with Bis(pinacolato)diboronâ M. A. Brimble and F. Issa, Australian Journal of Chemistry, 1999, 52, 1021-1028.
81. âDeprotonation and Alkylation of 2-Methyl-4,5,6,7-tetrahydrofuro-3H-azepineâ M. A. Brimble and S. Gorsuch, Australian Journal of Chemistry, 1999, 52, 965-969.
80. âSynthesis of Analogues of Griseusin Aâ M. A. Brimble, M. R. Nairn and J. Park, Organic Letters, 1999, 1, 1459-1462.
79. âAddition of a Grignard Reagent to Bis-Spiroacetal Aldehydes: Appendage of a Tetrahydrofuran Ringâ M. A. Brimble and H. Prabaharan, Journal of the Chemical Society, Perkin Transactions 1, 1999, 2795-2802.
78. âReactions of Semiquinones in Aqueous Solution. A Comparison of One Electron Reduction of Kalafungin and Analogues With Other Semiquinones Using Pulse Radiolysisâ R. F. Anderson, M. A. Brimble, M. R. Nairn and J. E. Packer, Journal of the Chemical Society, Perkin Transactions 2, 1999, 475-479.
77. âSynthetic Studies towards the B,C,D,E Fragment of Antibiotic CP44,161â P. A. Allen, M. A. Brimble, and H. Prabaharan, Synlett, 1999, 295-298.
76. âThe Synthesis of Oxygenated Naphthyl Stannanes Possessing ortho-Methoxy Substituents for use in Stille Coupling Reactionsâ M. A. Brimble and L. J. Duncalf, Australian Journal of Chemistry, 1999, 52, 19-29.
75. âDouble Furofuran Annulation to a Bis-Naphthoquinone: An Approach to Dimeric Pyranonaphthoquinonesâ M. A. Brimble, L. J. Duncalf and D. Neville, Journal of the Chemical Society, Perkin Transactions 1, 1998, 4165-4173.
74. âSynthesis of a Novel Cage Compound via Oxidative Rearrangement of a Dihydronaphthofuranâ M. A. Brimble, R. J. R. Elliott and P. Turner, Tetrahedron, 1998, 54, 14053-14058.
73. âSynthesis of Chiral Diazanedicarboxylatesâ M. A. Brimble, M. J. Duckworth and C. Y. K. Lee, Australian Journal of Chemistry, 1998, 51, 907-913.
72. âSynthesis of a Dimeric Pyranonaphthoquinone via a Novel Double Furofuran Annulation Strategyâ M. A. Brimble, D. Neville and L. J. Duncalf, Tetrahedron Letters, 1998, 39, 5647-5650.
71. âReductive Thioalkylation of a Kalafungin Analogueâ M. A. Brimble and M. R. Nairn, Tetrahedron Letters, 1998, 39, 4879-4882.
70. âSynthesis of C-2 Functionalised 1,6,8-Trioxadispiro[4.1.5.3]pentadec-13-enesâ M. A. Brimble, P. R. Allen and F. Fares, Journal of the Chemical Society, Perkin Transactions 1, 1998, 2403-2411.
69. âAddition of Cyclopentadiene and 2-Trimethylsilyloxyfuran to Quinones Bearing a Menthyl Ester Chiral Auxiliaryâ M. A. Brimble, L. J. Duncalf, D. C. W. Reid and T. R. Roberts, Tetrahedron, 1998, 54, 5363-5374.
68. âAsymmetric Michael Addition of 2-Trimethylsilyloxyfuran to Chiral Naphthoquinonesâ M. A. Brimble, J. F. McEwan and P. Turner, Tetrahedron Asymmetry, 1998, 9, 1257-1267.
67. âAsymmetric Diels-Alder Addition of Cyclopentadiene to Chiral Naphthoquinonesâ M. A . Brimble, J. F. McEwan and P. Turner, Tetrahedron Asymmetry, 1998, 9, 1239-1255.
66. âSynthesis of 7-Methoxy-3â,4â,5â,6â-tetrahydrospiro[isobenzofuran-1(3H),2â-pyran]-3-one and 5,7-Dimethoxy-3â,4â,5â,6â-tetrahydrospiro[isobenzofuran-1(3H),2â-pyran]-3-oneâ M. A. Brimble and S. Chan, Australian Journal of Chemistry, 1998, 51, 235-242.
65. âAsymmetric Azo-ene Reactions Using the Chiral Azo-Enophile Di-(â)-(1R,2S)-2-phenyl-1-cyclohexyl Diazenedicarboxylateâ M. A. Brimble and C. Y .K. Lee, Tetrahedron Asymmetry, 1998, 9, 873-884.
64. âApproaches to the D-E Ring of the Polyether Antibiotic Salinomycin Using Sharpless Asymmetric Dihydroxylationâ M. A. Brimble and H. Prabaharan, Tetrahedron, 1998, 54, 2113-2128.
63. âAddition of Allylsilanes to an Oxy-Stabilized Carbenium Ion on a 1,7-Dioxaspiro [5.5]-undecane Ring Systemâ M. A. Brimble, F. Fares and P. Turner, Journal of the Chemical Society, Perkin Transactions 1, 1998, 677-684.
62. âSynthesis of Crown Ethers Based on a Spiroacetal Frameworkâ M. A. Brimble and A. D. Johnston, Journal of the Chemical Society, Perkin Transactions 1, 1998, 265-270.
61. âSynthesis and Herbicidal Activity of [3R*,5S*,6S*]-3-Benzyloxy-5-methoxy-1,7-dioxaspiro[5.5]undecane and [3R*,5S*,6S*]-3-Methoxy-5-benzyloxy-1,7-dioxaspiro-[5.5]undecaneâ M. A. Brimble, R. J. Furneaux and A. D. Johnston, Journal of Organic Chemistry, 1998, 63, 471-479.
60. âUse of Bis(oxazoline)-Metal Complexes as Chiral Catalysts for Asymmetric Diels-Alder Reactions Using 2-Acetyl-1,4-naphthoquinone as Dienophileâ M. A. Brimble and J. F. McEwan, Tetrahedron Asymmetry, 1997, 8, 4069-4078.
59. âSynthesis of 8-Bromokalafungin as an Intermediate for the Preparation of C-Glycoside Derivativesâ
M. A. Brimble, M. R. Nairn, H. Prabaharan and N. B. Walters, Australian Journal of Chemistry, 1997, 50, 711-718.
58. âAddition of Silyloxydienes to 2-Substituted 1,4-Benzoquinones and 1,4-Naphthoquinonesâ M. A. Brimble and R. J. Elliott, Tetrahedron, 1997, 53, 7715-7730.
57. âKinetic Resolution in the Asymmetric Dihydroxylation of 1,7-Dioxaspiro[5.5]-undec-4-enesâ M. A. Brimble and A. D. Johnston, Tetrahedron Asymmetry, 1997, 8, 1661-1676.
56. âSynthesis of a New Spiroacetal Based Herbicideâ M. A. Brimble, R. J. Furneaux and A. D. Johnston, Tetrahedron Letters, 1997, 38, 3591-3594.
55. âSynthesis of the Monomeric Unit of gamma-Actinorhodinâ M. A. Brimble, L. J. Duncalf and S. J. Phythian, Journal of the Chemical Society, Perkin Transactions 1, 1997, 1399-1403.
54. âFacile Bisarylation of Aldehydes using Titanium Naphtholatesâ M. A. Brimble and E. Oppen, Synthetic Communications, 1997, 27, 989-1007.
53. âCrystal Structures of (3S*,4S*,5S*,6S*)-3,4-Epoxy-1,7-dioxaspiro[5.5]undecan-5-ol, (3R*,5S*,6S*)-1,7-Dioxaspiro[5.5]undec-3,5-diyl Diacetate and (4S*,5S*,6S*)-1,7-Dioxaspiro[5.5]undecan-4,5-diolâ M. A. Brimble, A. D. Johnston, T. W. Hambley and P. Turner, Australian Journal of Chemistry, 1997, 50, 123-127.
52. âSynthesis and Ene Reactions of Di-(â)-menthyl Diazenedicarboxylateâ M. A. Brimble, C. H. Heathcock and G. N. Nobin, Tetrahedron Asymmetry, 1996, 7, 2007-2016.
51. âSynthesis of Tricyclic Aryl Spiroacetals Related to the Papulacandinsâ M. A. Brimble and S. G. Robinson,
Tetrahedron, 1996, 52, 9553-9565.
50. âSynthesis of Spiroketals Related to Griseusin Aâ M. A. Brimble and M. R. Nairn, Molecules, 1996, 1, 3-14.
49. âWoodward-Prevost Reactions of 1,7-Dioxaspiro[5.5]undec-4-enesâ M. A. Brimble and M. R. Nairn, Journal of Organic Chemistry, 1996, 61, 4801-4805.
48. âSynthesis of Aromatic Spiroacetalsâ M. A. Brimble, G. M. Horner and R. J. Stevenson, Australian Journal of Chemistry, 1996, 49, 189-196.
47. âSynthesis of Chiral Hydroxylated Farnesene Derivativesâ M. A. Brimble, J. A. Spicer and D. D. Rowan, Synthesis, 1996, 116-122.
46. âSynthesis of (E)-1-Bromo-3-ethyl-3-penteneâ M. A. Brimble and M. K. Edmonds, Synthetic Communications, 1996, 26, 243-251.
45. âSynthesis of an Actinorhodin Monomerâ M. A. Brimble, L. J. Duncalf and S. J. Phythian, Tetrahedron Letters, 1995, 36, 9202-9210.
44. âSynthesis of Arizonin C1â M. A. Brimble, S. J. Phythian and H. Prabaharan, Journal of the Chemical Society, Perkin Transactions 1, 1995, 2855-2860.
43. âEnantioselective Synthesis of the Apple Aroma Constituent 1,3,3-Trimethyl-2,7-dioxabicyclo[2.2.1]heptane via Asymmetric Dihydroxylationâ M. A. Brimble, D. D. Rowan and J. A. Spicer, Synthesis, 1995, 1263-1266.
42. âSynthesis of Bis-2,5-linked Tetrahydrofurans via Iodoetherificationâ M. A. Brimble and M. K. Edmonds,
Tetrahedron, 1995, 51, 9995-10012.
41. âIdentification of Conjugated Triene Oxidation Products of alpha-Farnesene in Appleskinâ J. M. Allen, M. A. Brimble, S. Fielder, D. D. Rowan, and J. A. Spicer, Journal of Agriculture and Food Chemistry, 1995, 43, 2040-2045.
40. âDiastereoselective Addition of 2-Trimethylsilyloxyfuran to (S)-(+)-2-(p-Tolylsulfinyl)-1,4-benzoquinoneâ M. A. Brimble, L. J. Duncalf and D. C. W. Reid, Tetrahedron Asymmetry, 1995, 6, 263-269.
39. âAsymmetric Dihydroxylation of alpha- and beta-Farneseneâ M. A. Brimble, D. D. Rowan and J. A. Spicer, Tetrahedron Letters, 1994, 35, 9445-9446.
38. âFormal Synthesis of the Juglomycinsâ M. A. Brimble and E. Ireland, Journal of the Chemical Society, Perkin Transactions 1, 1994, 3109-3104.
37. âSynthesis of Conjugated Trienes and Related Oxidation Products of alpha-Farneseneâ M. A. Brimble, D. D. Rowan and J. A. Spicer, Australian Journal of Chemistry, 1994, 47, 1979-1988.
36. âDirected ortho Metallations of Tertiary Benzamides using Lactones as Electrophilesâ T. J. Brenstrum, M. A. Brimble and R. J. Stevenson, Tetrahedron, 1994, 50, 4897-4904.
35. âSynthesis of Bicyclic Pyrazinones via Addition of Heterocyclic Amines to a Nitro-alkeneâ M. A. Brimble and A. D. Johnston, Tetrahedron, 1994, 50, 4887-4896.
34. âSynthesis of trans- and cis-14-Phenylsulfonyl-1,7,9-trioxadispiro[5.1.5.3]hexadecaneâ M. A. Brimble and C. J. Rush, Journal of the Chemical Society, Perkin Transactions 1, 1994, 497-500.
33. âA Short Synthesis of Deoxyfrenolicinâ M. A. Brimble and S. M. Lynds, Journal of the Chemical Society, Perkin Transactions 1, 1994, 493-496.
32. âOxidation of alpha-Farneseneâ M. A. Brimble, D. D. Rowan and J. A. Spicer, Australian Journal of Chemistry, 1993, 46, 1929-1939.
31. âSynthesis of 5-epi-Arizonin B1 and 5-epi-Arizonin C1â M. A. Brimble and S. J. Phythian, Tetrahedron Letters, 1993, 34, 5813-5814.
30. âAllylic Amination by the Lewis-Acid-Mediated Ene Reaction of Diethyl Azodicarboxylate with Alkenesâ M. A. Brimble and C. H. Heathcock, Journal of Organic Chemistry, 1993, 58, 5261-5263.
29. âStructure of a Bis-Spiroacetal, cis-14-Phenylsulphonyl-1,7,9-trioxadispiro[5.1.5.3]hexadecaneâ E. N. Baker, M. A. Brimble, G. E. Norris, and C. J. Rush, Crystallographica, Section C: Crystal Structure Communications, 1993, 49, 1857-1859.
28. âDihydroxylation of 1,7-Dioxaspiro[5.5]undec-4-enesâ M. A. Brimble and M. R. Nairn, Australian Journal of Chemistry, 1993, 46, 195-201.
27. âSynthesis of the Bis-Spiroacetal Moiety of 17-epi-20-Deoxysalinomycinâ M. A. Brimble and G. M. Williams, Journal of Organic Chemistry, 1992, 57, 5818-5822.
26. âAllylic Functionalization of the 1,7-Dioxaspiro[5.5]undec-4-ene and 1,6,8-Trioxadispiro[4.1.5.3]pentadec-13-ene Ring Systemsâ M. A. Brimble, M. K. Edmonds, and G. M. Williams, Tetrahedron, 1992, 48, 6455-6466.
25. âSynthesis of Deuterated Hexenolsâ T. J. Brenstrum, M. A. Brimble, C. J. Rush, J. G. Shaw and D. C. W. Reid, Journal of Labelled Compounds and Radiopharmaceuticals, 1992, 8, 629-635.
24. âSynthesis of a Pyranonaphthoquinone-Spiroacetalâ M. A. Brimble and M. R. Nairn, Journal of the Chemical Society, Perkin Transactions 1, 1992, 579-583.
23. âSynthesis of 5′-Deoxyjuglomycin A and 5′-Methoxyjuglomycin Aâ M. A. Brimble, E. Ireland and S. J. Phythian, Tetrahedron Letters, 1991, 32, 6417-6420.
22. âChemistry of Bis-Spiroacetals: Synthesis of cis- and trans-1-(2-Methyl-1,6,8-trioxadispiro[4.1.5.3]pentadec-13-en-2-yl)methanolâ M. A. Brimble, G. M. Williams and R. Baker, Journal of the Chemical Society, Perkin Transactions 1, 1991, 2221-2227.
21. âHighly Stereoselective syn-Hydroxylation of Spiroketalsâ M. A. Brimble, M. R. Nairn and Y. Wu, Tetrahedron Letter, 1991, 32, 4049-4050.
20. âApproaches to a Key Lactone Intermediate Required for the Synthesis of Pyranonaphthoquinone Antibioticsâ M. A. Brimble and J. A. Spicer, Australian Journal of Chemistry, 1991, 44, 197-205.
19. âAllylic Oxidation of Unsaturated Spiroketalsâ M. A. Brimble, M. K. Edmonds and G. M. Williams, Tetrahedron Letters, 1990, 31, 7509-7512.
18. âSynthesis of a Functionalised Bis-Spiroacetalâ M. A. Brimble, G. M. Williams, R. Baker and M. James, Tetrahedron Letters, 1990, 31, 3043-3046.
17. âStereocontrolled Synthesis of a Key Lactone Intermediate Required for the Synthesis of Salinomycinâ M. A. Brimble, Australian Journal of Chemistry, 1990, 43, 1035-1046.
16. âThe Chemistry of Bis-Spiroacetals. Synthesis of the Novel 1,7,9-Trioxadispiro-[5.1.5.3]hexadecane Ring Systemâ M. A. Brimble, C. J. Rush, G. M. Williams and E. N. Baker, Journal of the Chemical Society, Perkin Transactions 1, 1990, 414-416.
15. âEffect of the Fungal Metabolite Peramine and Analogues on Feeding and Development of the Argentine Stem Weevil (Listronotus bonariensis)â M. A. Brimble, D. D. Rowan and J. J. Dymock, Journal of Chemical Ecology, 1990, 16, 1683-1695.
14. âSynthesis of 5-epi-7-Deoxykalafungin and 5-epi-7-O-Methylkalafunginâ M. A Brimble and S. J. Stuart, Journal of the Chemical Society, Perkin Transactions 1, 1990, 881-885.
13. âSynthesis of the Griseusin A Ring Systemâ M. A. Brimble and M. R. Nairn, Journal of the Chemical Society, Perkin Transactions 1, 1990, 169-171.
12. âSynthesis of the Insect Feeding Deterrent Peramine via Michael Addition of a Pyrrole Anion to a Nitroalkeneâ M. A. Brimble and D. D. Rowan, Journal of the Chemical Society, Perkin Transactions 1, 1990, 311-314.
11. âSynthesis of the cis-3a,8b-Dihydrofuro[3,2-b]benzofuran-2(3H)-one Ring System via a Furofuran Annulation to Activated Benzoquinonesâ M. A. Brimble, M. T. Brimble and J. J. Gibson, Journal of the Chemical Society, Perkin Transactions 1, 1989, 179-184.
10. âRearrangement of a Furo[3,2-b]naphtho[2,1-d]furan to a Pyranonaphthoquinoneâ M. A. Brimble, R. Hodges and S. J. Stuart, Tetrahedron Letters, 1988, 29, 5987-5990.
9. âSynthesis of Peramine: An Insect Feeding Deterrent Mycotoxin from Acremonium Loliiâ M. A. Brimble and D. D. Rowan, Journal of the Chemical Society, Chemical Communications, 1988, 978-979.
8. âSynthesis of 2-Methylpyrrolo[1,2-a]pyrazin-1(2H)-oneâ M. A. Brimble, M. T. Brimble, R. Hodges and G. A. Lane, Australian Journal of Chemistry, 1988, 41, 1583-1590.
7. âA Facile Synthesis of Spiroketalsâ M. A. Brimble, D. L. Officer and G. M. Williams, Tetrahedron Letters, 1988, 29, 3609-3612.
6. âThe Chemistry of Bis-Spiroacetals. Synthesis of the 1,6,8-Trioxadispiro[4.1.5.3]pentadecane Ring Systemâ R. Baker and M. A. Brimble, Journal of the Chemical Society, Perkin Transactions 1, 1988, 125-131.
5. â1,4-Addition of 2-Trimethylsilyloxyfuran to Quinones: A Facile Route to the Furo[3,2-b]benzofuran Nucleusâ M. A. Brimble, M. T. Brimble, J. J. Gibson, R. Baker, A. A. Kee and M. J. OâMahony, Tetrahedron Letters, 1987, 28, 4891-4892.
4. âSynthesis of Two Key Intermediates Required for the Construction of the Bis-Spiroacetal Moiety of epi-17-Deoxy-(O-8)-salinomycinâ R. Baker and M. A. Brimble, Tetrahedron Letters, 1986, 27, 3311-3314.
3. âDetermination of the Stereochemistry of 2,2-Dimethyl-1,6,8-trioxadispiro[4.1.5.3]pentadec-13-ene Formed by Two Sequential Cyclization Reactions Using High Field 1H NMR Spectroscopyâ R. Baker, M. A. Brimble, and J. A. Robinson, Tetrahedron Letters, 1985, 26, 2115-2118.
2. âThe Chemistry of Spiroacetals. Approaches to the Novel 1,6,8-trioxadispiro[4.1.5.3]pentadecane Ring Systemâ R. Baker and M. A. Brimble, Journal of the Chemical Society, Chemical Communications, 1985, 78-80.
1. âDiastereoselective Diels-Alder Reactions of Optically-Active Vinyl Sulphoxidesâ M. A. Brimble and B. R. Davis, Tetrahedron, 1985, 41, 4965-4971.
Non-Refereed Journals
30. âPreliminary Field Trials with a Palatable Form of Norbormideâ L. Shapiro, C. Eason, D. MacMorran, D. Rennison, M. A. Brimble and M. Jackson, Proceedings of the 29th Vertebrate Pest Conference, D. M. Woods Ed., 2020, paper 55, 1-3.
29. âThe Post-lockdown Period Should be Used to Acquire Effective Therapies for Future Resurgence in SARS-Cov-2 Infections,â K. L. Krause, R. Furneaux, P.Benjes, M. A. Brimble, T. Davidson, B. Denny, L. Harris, S. Hinkley, P. Tyler, J. Ussher and Vernon Ward, New Zealand Medical Journal, 24 April 2020, vol. 133, No. 1513, p107-111.
28. âRedevelopment of a Rat Specific Rodenticide Norbormideâ L. Shapiro, D. Rennison, M. A. Brimble, D. MacMorran and C. Eason, Proceedings of the 28th Vertebrate Pest Conference, D. M. Woods Ed., 2018, 47-50.
27. âGlobal Trends in the Development of Rodenticides and Mammalian Pest Control Technologiesâ C. Eason, W. Linklater, M. Jackson, L. Shapiro, H. Blackie, C.Morley, S. Olgivie, D. Rennison and M. A. Brimble, Proceedings of the 28th Vertebrate Pest Conference, D. M. Woods Ed., 2018, 3-10.
26. âOrganic Synthesis: Where to From Now? A Personal Perspective From Down Under,â M. A. Brimble, Organic Letters, 2019, 21, 5773-5774.
25. âCharacterising the Mode of Action of Connexin43 Mimetic Peptide5 to Target Retinal Ischemia-Reperfusion Injury,â Y. Kim, J. M. Griffin, P. W. R. Harris, S. H. C. Chan, L.F. B. Nicholson, S. J. O’Carroll, M. A. Brimble and C. Green, Investigative Ophthalmology & Visual Science, 2016, 57, 4592-4592.
24. âWeight Loss After Pregnancy is Associated with Reduced IGFBP-3 and Increased cGP/IGF-1 Ratioâ J. Guan, K. Liu, G. S. Mallah, L. McGowan, P. Shorten, J. Thompson, E. Mitchell, R. Taylor, P. Harris, M. A. Brimble and R. Murphy, Endocrine Abstracts, 2016, 41 EP709B | DOI:10.1530/endoabs.41.EP709B
23. âStrategies for Inhibiting Advanced Glycation Endproduct (Age) Induced Vascular Calcification in a Smooth Muscle Cell Culture Modeâ G. P. Sidgwick, P. Walling, A. Shabbir, R. Weston, A. Schiro, F. Serracino-Inglott, A. M. Jones, M. Kamalov, M. A. Brimble, F. L. Wilkinson and Y. Alexander, Heart, 2016, 102, Suppl 6, A132-A132. (IF = 6.0) DOI: 10.1136/heartjnl-2016-309890.196.
22. âTechnology Advances for Pest Eradicationâ C. Eason, L. Shapiro, J. Ross, E. Murphy, S. Olgivie, D. MacMorran, M. Jackson, K. Irie, S. M. Clout, D. Rennison and M. A. Brimble, Proceedings of the 27th Vertebrate Pest Conference, R. M. Timm and R. A. Baldwin, Eds., 2016, 390-395.
21. âDevelopment of New Chemical Probes for Investigation of the CB1-D2 Receptor Complexâ N. Kahlcke, D. Furkert, M. Glass and M. A. Brimble, FEBS Journal, 2015, 282(supplement), 403-403.
20. “A Novel IGF-II-like Synthetic Peptide for Improving Tendon Healing” D. S. Musson, M. L. Tay, G. W. Williams, K. E. Callon, B. Coleman, M. A. Brimble, J. Cornish, Tissue Engineering Part A, 2015, 21(supplement), S355-S356.
19. âRetaining or Retrieving Older and Trying to Identify Novel Rodenticidesâ C. Eason, E. Murphy, S. Sam, J. Ross, H. Blackie, R. Henderson, L. Shapiro, D. MacMorran, T. Gibson, N. Gregory, D. Conole, D. Rennison, and M. A. Brimble, Proceedings of the 25th Vertebrate Pest Conference, R. M. Timm Ed., 2012, 149-150.
18. âA Slow-gradient, Sample-displacement Chromatography Approach for the Purification of Synthetic Peptidesâ J. M. Wojnar, P. W. R. Harris and M. A Brimble, Biotech International, 2012, 24, 22-25.
17. âRetrieving and Retaining Older and Advancing Novel Rodenticides as Alternatives to Anticoagulantsâ C. T. Eason, R. Henderson, E. Murphy, L. Shapiro, D. MacMorran, H. Blackie, M. Brimble, D. Conole, D. Rennison, T. J. Gibson and N. G. Gregory, Proceedings of the 8th European Vertebrate Pest Management Conference, 2011, 19-20.
16. âDevelopment of NNZ-2566 as a Drug Candidate for Traumatic Brain Injury: The Neuren Storyâ M. A. Brimble and P. W. R. Harris, Chemistry in New Zealand, 2011, 75, 133-136. (Invited Paper from a Distinguished NZ scientist for Special Issue to Celebrate International Year of Chemistryâ)
15. âTrends in Vertebrate Pesticide Use and New Developments: New Zealand Initiatives and International Implicationsâ C. Eason, E. Murphy, S. Ogilivie, H. Blackie, J. Ross, M. Kaveramann, S. Sam, M. Statham, H. Statham, S. Lapidge, S. Humphrys, R. Henderson, D. MacMorran, T. Gibson, N. Gregory, J. Harrison, G. Giles, I. Summut, P. Jansen, D. Conole, D. Rennison, M. A. Brimble, Proceedings of 24th Vertebrate Pest Conference, 2010, 91-96.
14. âToxicodynamics of Methemoglobin (MetHb) Inducersâ C. Eason, M. A. Brimble, D. Rennison, M. D. Tingle, D. Conole, Proceedings of 24th Vertebrate Pest Conference, 2010, 108-114.
13. âChemistry Research: Making Molecules for Medicinesâ M. A. Brimble, p864-865 in Chemistry, J. W. Wiley and Sons Australia, Ltd., eds. A. Blackman, S. E. Bottle, S. Schmid, M. Mocerino and U. Wille, 2008, ISBN 9 78047081 0866 (pbk).
12. âScience of Synthesis, Volume 28: Compounds with Two CarbonâHeteroatom Bonds: Quinones and Heteroatom Analoguesâ Volume editor A. G. Griesbeck. Georg Thieme Verlag: Stuttgart, 2006, 1006 pp, hardback. ISBN 3-13-118791-3 (RoW); ISBN 1-58890-460-1 (US). Book review by M. A. Brimble, Synthesis, 2007, 18, 2924.
11. âEquipment Access for Graduate Students â The First Hurdleâ M. A. Brimble, Royal Society of New Zealand Alert Editorial, Issue 479, 5th July, 2007.
10. âProfessor Jim Coxon. A Tributeâ M. A. Brimble and P. Steel, Archive for Organic Chemistry (ARKIVOC), 2006, (iii), 1-5.
9. âSynthesis of Pharmaceuticals Using Molecular Chess and Automated Synthesisâ M. A. Brimble, Chemistry in New Zealand, 2004, 68, 5-9.
8. âTurning Toxins into Medicinesâ M.A. Brimble and M. S. Levi, Chemistry in New Zealand, 2003, 66, No. 93, 18-24.
7. âPushing Out Research Boundaries in Medicinal Chemistryâ M. A. Brimble, New Zealand Pharmacy, 2002, 3, 15.
6. âSynthetic Studies Towards Natural Products Containing Bis-Spiroacetalsâ M. A. Brimble, Federation of Asian Chemical Societies Journal, 2002, 12-15.
5. âThe Synthesis of Potential Chemotherapeutic Agents based on Leads from Natureâ M. A. Brimble, Federation of Asian Chemical Societies Journal, 2001, 24-28.
4. âThe Synthesis of Potential Chemotherapeutic Agents based on Leads from Natureâ M. A. Brimble, Chemistry in Australia, 2001, 68, 15-17.
3. “Synthesis of Biologically Active Natural Products” M.A. Brimble, Chemistry in New Zealand, 1995, 58, 15-18.
2. “Apple Scald: Unravelling the Chemistry” M.A. Brimble, P. F. Reay, D. D. Rowan and J. A. Spicer, Chemistry in New Zealand, 1994, 58, 29-30.
1. “Strategic Synthesis : Science or Service” M.A. Brimble and D. D. Rowan, Chemistry in New Zealand, 1993, 57, 6-8.
96. âAn Insight into FDA Approved Antibody-Drug Conjugates for Cancer
Therapy,â J. T. W. Tong, P. W. R. Harris, M. A. Brimble and I. Kavianinia, Molecules, 2021, 26, 5847-5870. https://doi.org/10.3390/molecules26195847 (IF = 4.4) (Invited Article for Special Edition on Advances in Anticancer Drug Discovery II)
95. âCyclic Peptide Natural Products Cross-linked via the Tryptophan Side Chain,â J. A. Swain, S. Walker, M. B. Calvert and M. A. Brimble, Natural Product Reports, 2021, 38, doi: 10.1039/D1NP00043H (IF = 11.9)
94. âAminovinyl Cysteine Containing Peptides: A Unique Motif That Imparts Key Biological Activity,â
E. S. Grant-Mackie, E. T. Williams, P. W. R. Harris and M. A. Brimble, Journal of the American Chemical Society Au, 2021, in press. (IF = 12.35) (Invited Article)
93. âDevelopment of Peptide-Based Antibiotics,â C. C. Hanna, Y. O. Hermant, P. W. R. Harris and M. A. Brimble, Accounts of Chemical Research,â 2021, 54, 1878â1890. (IF = 21.7) (Invited Article for Special Issue dedicated to the topic of Bacterial Multi-Drug Resistance, Guest Editors: Ryan Looper and Dale L. Boger)
92. âFluorescent Probes for Bioimaging of Potential Biomarkers in Parkinsonâs Disease,â L. Gao, W. Wang, X. Wang, F. Yang, L. Xie, J. Shen, M. A. Brimble, Q. Xiao and S. Yao, Chemical Society Reviews, 2021, 50, 1219-1250. (IF = 42.8)
91. âseco-Labdanes: a Study of Terpenoid Structural Diversity Resulting from Biosynthetic CâC Bond Cleavage,â P. S. Grant and M. A. Brimble, Chemistry: A European Journal, 2021, 27, 6367-6389. (IF = 5.2)
90. âPhotoinduced ThiolâEne Chemistry: A Versatile Toolbox for Peptide-Based Drug Design,â M. Ahangarpour, I. Kavianinia, P. W. R. Harris and M. A. Brimble, Chemical Society Reviews, 2021, 50, 898-944. (IF = 42.8) (Selected for Outside Back Cover Image)
89. âBuilding trans-Bicyclo[4.4.0]decanes/decenes in Complex Multifunctional Frameworks: The Case for Antibiotic Development,â W. Zhang, A. R. Kaplan, E. K. Davison, J. L. Freeman, M. A. Brimble and W. M. Wuest, Natural Product Reports, 2020, 37, in press. https://doi.org/10.1039/D0NP00052C (IF = 11.9)
88. âThe Synthesis and Bioactivity of the Marine Macrolide Callyspongiolide,â K.-Y. Ko, Z. E. Wilson and M. A. Brimble, Chemistry: A European Journal, 2020, 26, in press. https://doi.org/10.1002/chem.202003898 (IF = 5.2)
87. âIdentification of Key Functional Motifs of Native Amelogenin Protein for Dental Enamel Remineralisation,â S. S. M. Dissanayake, M. Ekambaram, K. C. Li, P.W. R. Harris and M. A. Brimble, Molecules, 2020, 25, 4214-4223. https://doi.org/10.3390/molecules25184214 (IF = 3.3) ⢠(Special Issue for Women in Bioorganic Chemistry)
86. Chapter 3, âApplications of C-H Activation on Macromolecules (Peptides),â Z. Wilson and M. A. Brimble in C-H Activation Primer for Nature Reviews Methods Primer, L. Ackermann and S. Paiva (Eds), Nature Research, London. ⢠(Invited Chapter)
85. âEvolution of Peptide-Based Prostate-Specific Membrane Antigen (PSMA) Inhibitors: An Approach to Novel Prostate Cancer Therapeutics,â A. Siow, R. Kowalczyk, P. W. R. Harris and M. A. Brimble, Current Medicinal Chemistry, 2020, in press. https://doi.org/10.2174/0929867327666201006153847 (IF = 4.2)
84. âEnzymatic and Non-Enzymatic Crosslinks Found in Collagen and Elastin and Their Chemical Synthesis,â J. M. Gaar, R. Naffa and M. A. Brimble, Organic Chemistry Frontiers, 2020, 7, 2789-2814. https://doi.org/10.1039/D0QO00624F (IF = 5.2) ⢠(Selected for Front Cover Image)
83. âent-Atisane Diterpenoids: Isolation, Structure, and Bioactivity,â G. J. Drummond, P. S. Grant and M. A. Brimble, Natural Product Reports, 2020, 37, https://doi.org/10.1039/D0NP00039F (IF = 11.9)
82. âSynthesis of Lipopeptides by CLipPA Chemistry,â V. Yim, Y. O. Hermant, P. W. R. Harris and M. A. Brimble in Peptide Conjugation â Methods and Protoculs in Methods in Molecular Biology, 2020. W. M. Hussein, R. Stephenson, I. Toth (eds), Springer Nature, Humana Press, New York. ⢠(Invited Chapter) 81. âRecent Progress in the Synthesis of Homogeneous Erythropoietin (EPO) Glycoforms,â Y. Wang, S.-H. Yang, P. W. R. Harris and M. A. Brimble, ChemBioChem, 2020, https://doi.org/10.1002/cbic.202000347 (IF = 2.6) ⢠(VIP Article)
80. âTLR2 Agonists and their Structure-Activity Relationships,â B. L. Lu, G. M. Williams and M. A. Brimble, Organic and Biomolecular Chemistry, 2020, 18, 5073-5094. https://doi.org/10.1039/D0OB00942C (IF = 3.6)
79. âMolecules derived from the Extremes of Life: A Decade Later,â Z. E. Wilson and M. A. Brimble, Natural Product Reports, 2020, 37, https://doi.org/10.1039/D0NP00021C. (IF = 11.9)
78. âSynthetic Approaches Towards Bedaquiline and its Derivatives,â M. B. Calvert, D. P. Furkert, C. B. Cooper and M. A. Brimble, Bioorganic and Medicinal Chemistry Letters, 2020, 30, 12712-12782. https://doi.org/10.1016/j.bmcl.2020.127172 (IF = 2.4) ⢠(Invited Review)
77. âNorbormide-based Probes and their Application for Mitochondrial Imaging in Drosophila Melanogaster,â A. Forgiarini, Z. Wang, S. Bova, M. A. Brimble, B. Hopkins, D. Rennison and G. Orso in Mitochondrial Medicine: Methods and Protocols, Second Edition, 2020, vol., in press. V Weissig and M. Edeas (eds), Springer Nature, Humana Press, New York. Mito Medicine due for release April 20th 2021 https://www.springer.com/gp/book/9781071612699
76. âSynthetic Studies towards Spiroimine Marine Toxins using N-Acyl Iminium Ions as Dienophiles in Diels-Alder Reactions,â J. L. Freeman, F. F. Li, D. P. Furkert and M. A. Brimble, Synlett, 2020, 31, 657-671. http://doi.org/10.1055/s-0039-1691593 (IF = 2.4) ⢠(Invited Review and Highlight Article)
75. âNaturally Occurring Antitubercular Cyclic Peptides,â S. Zhang, I. Kavianinia and M. A. Brimble, Tetrahedron Letters, 2019, 60, 151399-151352. https://doi.org/10.1016/j.tetlet.2019.151339 (IF = 2.4) ⢠(Invited Review)
74. âBenzannulated Spiroketal Natural Products: Isolation, Biological Activity, Biosynthesis, and Total Synthesis,â R. Gillard and M. A. Brimble Organic and Biomolecular Chemistry, 2019, 17, 8272-8307. https://doi.org/10.1039/C9OB01598A (IF = 3.6)
73. âNaturally Occurring Lumazines,â B. J. Daniels, F. F. Li, D. P. Furkert and M. A. Brimble, J. Natural Products, 2019, 82, 2054-2065. https://doi.org/10.1021/acs.jnatprod.9b00351 (IF = 4.3)
72. âThree Decades of Amyloid Beta Synthesis: Challenges and Advances,â J. K. Kasem, P. W. R. Harris, I. Kavianinia and M. A. Brimble, Frontiers in Chemistry – Chemical Biology, 2019, 02 July 2019, https://doi.org/10.3389/fchem.2019.00472 (IF = 3.8) ⢠(Invited Review)
71. âSynthesis of Antimicrobial Lipopeptides Using the âCLipPAâ Thiol-ene Reaction,â Y. O. Hermant, A. J. Cameron, P. W. R. Harris and M. A. Brimble in Peptide Synthesis â Methods and Protoculs in Methods in Molecular Biology, 2020, vol 2103. W. Hussein, M. Skwarczynski, I. Toth (eds), Springer Nature Protoculs, Humana Press, New York. https://doi.org/10.1007/978-1-0716-0227-0_18 ⢠(Invited Chapter)
70. âVery Short and Stable Lactoferricin Derived Antimicrobial Peptides: Design Principles and Potential Uses,â J. Svendsen, T. Grant, D. Rennison, M. A. Brimble and J. Svenson, Accounts of Chemical Research, 2019, 52, 749-759. https://doi.org/10.1021/acs.accounts.8b00624 (IF = 21.0) ⢠(Invited Review)
69. âUsing Chemical Synthesis to Optimise Antimicrobial Peptides in the Fight against Antimicrobial Resistance,â Pure and Applied Chemistry, F. F. Li and M. A. Brimble, 2019, 91, 181-198. https://doi.org/10.1515/pac-2018-0704 (IF = 5.3) ⢠(Invited Special Issue for Distinguished Women in Chemistry and Chemical Engineering)
68. âNatural Product Derived Privileged Scaffolds in Drug Discovery,â E. K. Davison and M. A. Brimble, Current Opinion in Chemical Biology, 2019, 52, 1-8. https://doi.org/10.1016/j.cbpa.2018.12.007 (IF = 7.6)
67. â2âFormylpyrrole Natural Products: Origin, Structural Diversity, Bioactivity and Synthesisâ J. M. Wood, D. P. Furkert and M. A. Brimble, Natural Product Reports, 2019, 36, 289-306. https://doi.org/10.1039/C8NP00051D (IF = 11.4)
66. âChemical Synthesis of Bioactive Naturally Derived Cyclic Peptides Containing Ene-Like Rigidifying Motifsâ L. M. De Leon Rodriguez, E. T. Williams and M. A. Brimble, Chemistry: A European Journal, 2018, 24, 17869-17880. https://doi.org/10.1002/chem.201802533 (IF = 5.3) ⢠(Invited Frontispiece Colour Image)
65. âA New Family of Sesterterpenoids Isolated Around The Pacific Rimâ H. J. Shirley, M. L. Jamieson, M. A. Brimble and C. D. Bray, Natural Product Reports, 2018, 35, 210-219. https://doi.org/10.1039/C7NP00049A (IF = 11.4) ⢠(Front Cover. Featured in Royal Society of Chemistry themed collection âCelebrating Excellence in Research: 100 Women of Chemistry)
64. âSynthesis of N-Linked Glycopeptides Using Convergent Enzymatic Glycosylation Combined with SPPSâ R. Kowalczyk, H. Kaur, A. J. Fairbanks and M. A. Brimble, in Coupling and Decoupling of Diverse Molecular Units in Glycoscience, 2018, p1-36. Z. J. Witczak and R. Bielski (Eds), Springer International Publishing, Cham, Switzerland. https://doi.org/10.1007/978-3-319-65587-1_1 ⢠(Invited Book Chapter).
63. âPeptide Lipidation â A Synthetic Strategy to Afford Peptide Based Therapeuticsâ R. Kowalczyk, P. W. R. Harris, G. M. Williams, S.-H. Yang and M. A. Brimble, in Peptides and Peptide-based Biomaterials and their Biomedical Applications. Advances in Experimental Medicine and Biology, 2017, vol 1030, p185-227. A. Sunna, A. Care and P. Bergquist (Eds.), Springer International Publishing, Cham, Switzerland. https://doi.org/10.1007/978-3-319-66095-0_9 ⢠(Invited Book Chapter).
62. âSynthesis of Enediamino Amino Acid Analogues and Peptidesâ S. Zhang, L. M. De Leon Rodriguez, P. W. R. Harris and M. A. Brimble, Asian Journal of Organic Chemistry, 2017, 6, 1180-1190. https://doi.org/10.1002/ajoc.201700169 (IF = 3.3) ⢠(Invited Review for Special Issue for Editorial Advisory Board Members and Cover Image)
61. âSynthesis of AHMOD-containing Aminolipopeptides, Unique Bioactive Peptaibioticsâ L. A. Stubbing, I. Kavianinia and M. A. Brimble, Organic and Biomolecular Chemistry, 2017, 15, 3542-3549. https://doi.org/10.1039/C7OB00541E (IF = 3.6)
60. âGold Catalysis: Synthesis of Spiro, Bridged, and Fused Ketal Natural Productsâ R. Quach, D. P. Furkert and M. A. Brimble, Organic and Biomolecular Chemistry, 2017, Organic and Biomolecular Chemistry, 3098-3104. https://doi.org/10.1039/C7OB00496F (IF = 3.6) ⢠(Front Cover and Invited Review)
59. âGaq Proteins: Molecular Pharmacology and Therapeutic Potentialâ D. Kamato, P. Mitra, F. Davis, N. Osman, R. Chaplin, P. J. Cabot, R. Afroz, W. Thomas, W. Zheng, H. Kaur, M. A. Brimble and P. J. Little, Cell and Molecular Life Sciences, 2017, 74, 1379-1390. https://doi.org/10.1007/s00018-016-2405-9 (IF = 5.8)
58. âPyranonaphthoquinones â Isolation, Biology and Synthesis: An Updateâ B. J. Naysmith, P. A. Hume, J. Sperry and M. A. Brimble, Natural Product Reports, 2017, 34, 25-61. https://doi.org/10.1039/C6NP00080K (IF = 11.0)
57. âEnduracididine, a Rare Amino Acid Component of Peptide Antibiotics: Natural Products and Synthesisâ D. J. Atkinson, B. J. Naysmith, D. P. Furkert and M. A. Brimble, Beilstein Journal of Organic Chemistry, 2016, 12, 2325-2342. https://doi.org/10.3762/bjoc.12.226 (IF = 2.7) ⢠(Invited Review for Special Issue âNatural Products in Synthesis and Biosynthesis II edited by Jeroen S. Dickshat)
56. âChemical Synthesis of Peptides Containing Site-Specific Advanced Glycation Endproductsâ H. Kaur, M. Kamalov and M. A. Brimble, Accounts of Chemical Research, 2016, 49, 2199-2208. https://doi.org/10.1021/acs.accounts.6b00366 (IF = 22.3) ⢠(Invited Review)
55. âStructureâMechanical Property Correlations of Hydrogel Forming beta-Sheet Peptidesâ L. M. De Leon Rodriguez, Y. Hemar, J. Cornish and M. A. Brimble, Chemical Society Reviews, 2016, 45, 4797-4824. https://doi.org/10.1039/C5CS00941C (IF = 33.4).
54. âShort Anabolic Peptides for Bone Growthâ Z. Amso, J. Cornish and M. A. Brimble, Medicinal Research Reviews, 2016, 36, 579-640. https://doi.org/10.1002/med.21388 (IF = 8.4)
53. âNitropyrrole Natural Products: Isolation, Biosynthesis and Total Synthesisâ X.-B. Ding, M. A. Brimble and D. P. Furkert, Organic and Biomolecular Chemistry, 2016, 14, 5390-5401. https://doi.org/10.1039/C5OB02599K (IF = 3.6)
52. âIntermolecular Peptide Cross-linking by Using Diaminodicarboxylic Acidsâ M. Kamalov, H. Kaur and M. A. Brimble, Chemistry – A European Journal, 2016, 22, 3622-3631 https://doi.org/10.1002/chem.201503458 (IF = 5.7) ⢠(Front Cover and Invited Review for Special Issue âWomen in Chemistryâ to celebrate International Womenâs Day 2016. To view the complete issue)
51. âSynthesis and Bioactivity of Antitubercular Peptides and Peptidomimetics: An Updateâ L. M. De Leon Rodriguez, H. Kaur and M. A. Brimble, Organic and Biomolecular Chemistry, 2016, 14, 1177-1187. https://doi.org/10.1039/C5OB02298C (IF = 3.6)
50. âAn Update on New Methods to Synthesize Cyclotetrapeptidesâ L. M. De Leon Rodriguez, A. J. Weidkamp and M. A. Brimble, Organic and Biomolecular Chemistry, 2015, 13, 6906-6921. https://doi.org/10.1039/C5OB00880H (IF = 3.6)
49. âTotal Synthesis of the Fungal Metabolite Virgatolide Bâ P. A. Hume, D. P. Furkert and M. A. Brimble in Strategies and Tactics in Organic Synthesis, STOS Volume 11, ed. M. Harmata, Elsevier Ltd., London, 2015, 119-150. ISBN: 978-0-08-100023-6; ISSN: 1874-6004. https://doi.org/10.1016/B978-0-08-100023-6.00005-1 ⢠(Invited Review)
48. âIsolation, Biological Activity, Biosynthesis and Synthetic Studies Towards the Rubromycin Family of Natural Productsâ D. J. Atkinson and M. A. Brimble, Natural Product Reports, 2015, 32, 811-840. https://doi.org/10.1039/C4NP00153B (IF = 10.7)
47. âStructure, Function, Pharmacology and Therapeutic Potential of the G Protein, GÎą/q,11â D. Kamato, L. Thach, R. Bernard, V. Chan, W. Zheng, H. Kaur, M. A. Brimble, N. Osman and P. J. Little, Frontiers in Cardiovascular Medicine, 2015, 2, 1-11. https://doi.org/10.3389/fcvm.2015.00014 (IF = 3.9)
46. âThe Role for IGF-1-derived Small Neuropeptides as a Therapeutic Target for Neurological Disordersâ J. Guan, P. W. R. Harris, M. A. Brimble, Y. Lei, J. Lu, Y. Lei, J. Lu, Y. Yang and A. J. Gunn, Expert Opinion on Therapeutic Targets, 2015, 19, 785-793. https://doi.org/10.1517/14728222.2015.1010514 (IF = 4.9)
45. âA Review of the Synthesis of alpha-Carbolinesâ A. D. Wadsworth, B. J. Naysmith and M. A. Brimble, European Journal of Medicinal Chemistry, 2015, 97, 816-829. https://doi.org/10.1016/j.ejmech.2014.11.038 (IF = 4.1)
44. âEnhancing the Oral Bioavailability of Peptide Drugs by using Chemical Modification and Other Approachesâ N. Yin, M. A. Brimble, P. W. R. Harris and J. Wen, Medicinal Chemistry, 2014, 4, 763-769. http://doi.org/10.4172/2161-0444.1000227 (Index Copernicus = 79.83)
43. âRecent Developments in Transition Metal-Catalysed Spiroketalisationâ R. Quach, D. F. Chorley and M. A. Brimble, Organic and Biomolecular Chemistry, 2014, 12, 7423-7432. https://doi.org/10.1039/C4OB01325E (IF = 3.6) ⢠(Invited Review)
42. âC-H Functionalization in the Synthesis of Amino Acids and Peptidesâ A. Noisier and M. A. Brimble, Chemical Reviews, 2014, 114, 8775-8806. https://doi.org/10.1021/cr500200x (IF = 45.7) ⢠(Invited Review)
41. âGlucose as an Agent of Post-translational Modification in Diabetes – New Cardiac Epigenetic Insightsâ K. M. Mellor, M. A. Brimble and L. M. D. Delbridge, Life Sciences, 2015, 129, 48-53. https://doi.org/10.1016/j.lfs.2014.03.020 (IF = 2.6)
40. âSynthesis of 5,6- and 6,6-Spirocyclic Compoundsâ M. A. Brimble and L. A. Stubbing in Topics in Heterocyclic Chemistry: Synthesis of Saturated Oxygen Heterocycles I, ed. J. Cossy, Springer-Verlag, Berlin Heidelberg, 2014, 35, 189-267. ISSN: 1861-9282; ISSN: 1861-9290 (electronic); ISBN: 978-3-642-41472-5; ISBN: 978-3-642-41473-2 (eBook); https://doi.org/10.1007/978-3-642-41473-2 ⢠(Invited Review)
39. âRules for the Abbreviation of Protecting Groupsâ M. A. Brimble, D. StC. Black, R. Hartshorn, A. P. Rauter, C.-K. Sha and L. V. Sydnes, Pure and Applied Chemistry, 2013, 85, 307-313. https://doi.org/10.1351/PAC-REP-12-07-12 (IF = 3.4) ⢠(IUPAC Technical Report)
38. âN-Alkylsulfonylimines as Dipolarophiles in Cycloaddition Reactionsâ L. A. Stubbing, G. P. Savage and M. A. Brimble, Chemistry – An Asian Journal, 2013, 8, 42-48. https://doi.org/10.1002/asia.201200584 (IF = 4.6)
37. âNeoglycoprotein Synthesis using the Copper-Catalyzed Azide-Alkyne Click Reaction and Native Chemical Ligationâ J. M. Wojnar, D. J. Lee, C. W. Evans, K. Mandal, S. B. Kent and M. A. Brimble, in Click Chemistry in Glycoscience – New Developments and Strategies, Bielski and Witczak (Ed.), Wiley-VCH, Hoboken, New Jersey, 2013, p253-270. ISBN 978-1-118-27533-7. https://doi.org/10.1002/9781118526996.ch10 ⢠(Invited Book Chapter)
36. âThe Kulinkovich Hydroxycyclopropanation Natural Product Synthesisâ I. Haym and M. A. Brimble, Organic and Biomolecular Chemistry, 2012, 10, 7649-7665. https://doi.org/10.1039/c2ob26082d (IF = 3.6) ⢠(Invited Review – selected for âFront Coverâ)
35. âSynthesis of Glycosylated 5-Hydroxylysine, an Important Amino acid present in Collagen-like Proteins such as Adiponectinâ K. R. Herbert, G. M. Williams, G. J. S. Cooper and M. A. Brimble, Organic and Biomolecular Chemistry, 2012, 10, 1137-1144. https://doi.org/10.1039/C1OB06394D (IF = 3.6)
34. âSynthetic Approaches to [5,6]-Benzannulated Spiroketal Natural Productsâ M. C. McLeod, M. A. Brimble, D. C. K. Rathwell, Z. E. Wilson and T.-Y. Yuen, Pure and Applied Chemistry, 2012, 84, 1379-1390. https://doi.org/10.1351/PAC-CON-11-08-06 (IF = 3.4)
33. âSynthesis of Dehydrotryptophan and Dehydrotrytophan-Containing Peptidesâ H. Kaur, A. Heapy and M. A. Brimble, Organic and Biomolecular Chemistry, 2011, 9, 5897-5907. https://doi.org/10.1039/c1ob05777d (IF = 3.7) ⢠(Highlighted on the Organic and Biomolecular Chemistry blog at http://blogs.rsc.org/ob/ and promoted through the OBC Twitter account http://twitter.com/OrgBiomolChem.)
32. âNatural Products Targeting Telomere Maintenanceâ J. L.-Y. Chen, J. Sperry, N. Y. Ip and M. A. Brimble, MedChemComm, 2011, 2, 229-245. https://doi.org/10.1039/C0MD00241K (IF = 2.8) ⢠(Invited Review for Inaugural Issue)
31. âSynthetic Studies Towards the Spiroimine Unit of the Spirolidesâ S. Gueret and M. A. Brimble, Pure and Applied Chemistry, 2011, 83, 425-433. https://doi.org/10.1351/PAC-CON-10-09-12 (IF = 2.8)
30. âRecent Developments in Neoglycopeptide Synthesisâ M. A. Brimble, N. Miller and G. M. Williams, in Amino Acids, Peptides and Proteins in Organic Chemistry. Volume 4 â Protection Reactions, Medicinal Chemistry, Combinatorial Synthesis, A.B. Hughes (Ed.), ISBN: 978-3-527-32103-2, Wiley-VCH, Weinham, Germany, 2011, 359-392. https://doi.org/10.1002/9783527631827.ch11 ⢠(Invited Review)
29. âSynthesis and Antifreeze Activity of Fish Antifreeze Glycoproteins and their Analogues,” R. Peltier, M. A. Brimble, J. M. Wojnar, D. E. Williams, C. W. Evans, A. L. DeVries, Chemical Science, 2010, 1, 538-551. https://doi.org/10.1039/C0SC00194E (IF = 7.5) ⢠(Invited Review for Inaugural Issue)
28. âSpiroimine Shellfish Poisoning (SSP) and the Spirolide Family of Shellfish Toxins: Isolation, Structure, Biological Activity and Synthesisâ S. GuĂŠret and M. A. Brimble, Natural Product Reports, 2010, 27, 1350-1366. https://doi.org/10.1039/C005400N (IF = 9.8)
27. âIsolation, Biological Activity and Synthesis of Benzannulated Spiroketal Natural Productsâ J. Sperry, Z. E. Wilson, D. C. K. Rathwell and M. A. Brimble, Natural Product Reports, 2010, 27, 1117-1137. https://doi.org/10.1039/B911514P (IF = 9.8) ⢠(Invited Review – for a thematic series called âSynthetic Natural Product Chemistryâ)
26. âSynthesis of Neoglycopeptides via Click Chemistryâ N. Miller, G. M. Williams and M. A. Brimble, International Journal of Peptide Research and Therapeutics, 2010, 16, 125-132. http://doi.org/10.1007/s10989-010-9201-4 (IF = 1.0) ⢠(Invited Review)
25. âMethyltrichlorosilane, CAS No: 75-79-6 Updateâ M. A. Brimble, Electronic Encyclopedia of Reagents for Organic Synthesis [e-EROS], eds. L. A. Paquette, D. Crich, P. L. Fuchs and P. Wipf, John Wiley & Sons Inc., 2010; Handbook of Reagents for Organic Synthesis: Reagents for Silicon-Mediated Organic Synthesis, ed. P. L. Fuchs, 2011, 389-393. https://doi.org/10.1002/047084289X.rm265.pub2
24. âSynthesis of Natural Products Containing Spiroketals via Intramolecular Hydrogen Abstractionâ J. Sperry, Y.-C. Liu and M. A. Brimble, Organic and Biomolecular Chemistry, 2010, 8, 29-38. https://doi.org/10.1039/B916041H (IF = 3.7) ⢠(Invited Review and Top 10 Downloaded Articles)
23. âMolecules Derived from the Extremes of Lifeâ Z. E. Wilson and M. A. Brimble, Natural Product Reports, 2009, 26, 44-71. https://doi.org/10.1039/b800164m (IF = 9.8) ⢠(Invited Review – selected for âFront Coverâ, also featured in âExtreme Potentialsâ Chemistry World, 2011, 8(6), 48-51.)
22. âInstant Insight: Life at the Extremesâ Z. E. Wilson and M. A. Brimble, Chemistry World, 2008, 5(12), 29-30. https://doi.org/10.1039/B819246B
21. âPyrans and Benzo Derivatives: Synthesisâ M. A. Brimble, J. Sperry and J. S. Gibson, Comprehensive Heterocyclic Chemistry III, eds. A. R. Katritzky, C. A. Ramsden, E. F. V. Scriven and R. J. K. Taylor, Elsevier, Oxford, 2008, 7, 419-700. http://dx.doi.org/10.1016/B978-008044992-0.00608-8
20. âPyranonaphthoquinonesâIsolation, Biological Activity and Synthesisâ J. Sperry, P. Bachu and M. A. Brimble, Natural Product Reports, 2008, 25, 376-400. https://doi.org/10.1039/b708811f (IF = 9.8) ⢠(Invited Review – selected for inclusion in Chemical Biology, 2008, issue 5)
19. â2-Trimethylsilyloxyfuran, CAS No: 61550-02 Updateâ J. Sperry and M. A. Brimble, Electronic Encyclopedia of Reagents for Organic Synthesis [e-EROS], eds. L. A. Paquette, D. Crich, P. L. Fuchs and P. Wipf, John Wiley & Sons Inc., 2007; Handbook of Reagents for Organic Synthesis: Reagents for Silicon-Mediated Organic Synthesis, ed. P. L. Fuchs, 2011, 684-693. http://doi.org/10.1002/047084289X.rt327.pub2
18. âUse of Stabilized Phthalide Anion Annulation Reactions in Synthesis: An Updateâ K. Rathwell and M. A. Brimble, Synthesis, 2007, 643-662. http://doi.org/10.1055/s-2007-965915 (IF = 2.5) ⢠(Invited Review)
17. âSynthesis of Macrocyclic Shellfish Toxins Containing Spiroimine Moietiesâ P. D. OâConnor and M. A. Brimble, Natural Product Reports, 2007, 24, 869-885. https://doi.org/10.1039/B700307M (IF = 9.8) ⢠(Invited Review)
16. âSynthetic Studies Towards Shellfish Toxins Containing Spiroacetal Unitsâ M. A. Brimble and R. Halim, Pure and Applied Chemistry, 2007, 79, 153-162. https://doi.org/10.1351/pac200779020153 (IF = 2.8)
15. âPolyether Antibioticsâ M. A. Brimble, Kirk-Othmer Encyclopedia of Chemical Technology, 5th Edition, ed. A. Seidel, John Wiley & Sons, Inc., 2006, 20, 119-148. https://doi.org/10.1002/0471238961.1615122503180114.a01.pub2 ⢠(Invited Review)
14. âSynthetic Studies Towards the Pectenotoxins: A Reviewâ M. A. Brimble and R. Halim, Organic and Biomolecular Chemistry, 2006, 4, 4048-4058. https://doi.org/10.1039/B611531B (IF = 3.7)
13. âA Review of Agents Patented for their Neuroprotective Propertiesâ M. A. Brimble and M. S. Levi, Recent Patents in CNS Drug Discovery, 2006, 1, 139-146. https://doi.org/10.2174/157488906777452758
12. âA Review of Neuroprotective Agentsâ M. A. Brimble and M. S. Levi, Frontiers in Medicinal Chemistry, eds. A. B. Reitz and Atta-ur-Rahman, Bentham Science, Karachi, 2006, 3, 163-194. https://doi.org/10.2174/978160805206610603010163
11. âA Review of Advances in the Synthesis of Analogues of the Delphinium Alkaloid Methyllycaconitineâ K. J. Goodall, D. Barker and M. A. Brimble, Synlett, 2005, 1809-1827. http://dx.doi.org/10.1055/s-2005-871575 (IF = 2.7)
10. âAlkylarsenic, -antimony, and -bismuth Compoundsâ M. A. Brimble and M. S. Levi, Comprehensive Organic Functional Group Transformations II, eds. A. R. Katritzky and R. J. K. Taylor, Elsevier Ltd., Oxford, 2005, 2, 463-484. https://doi.org/10.1016/B0-08-044655-8/00031-3
9. âA Review of Neuroprotective Agentsâ M. A. Brimble and M. S. Levi, Current Medicinal Chemistry, 2004, 11, 2383-2398. https://doi.org/10.2174/0929867043364522 (IF = 4.9)
8. âPolyether Antibioticsâ M. A. Brimble, Kirk-Othmer Encyclopedia of Chemical Technology Online Edition, ed. A. Seidel, John Wiley & Sons, Inc., 2003. https://doi.org/10.1002/0471238961.1615122503180114.a01.pub2 ⢠(Invited Review)
7. âChemistry of Bis-Spiroacetal Systems: Natural Products, Synthesis and Stereochemistryâ M. A. Brimble and D. P. Furkert, Current Organic Chemistry, 2003, 7, 1461-1484. http:// doi.org/10.2174/1385272033486404 (IF = 3.1)
6. âDi-(â)-(1R,2S)-2-phenyl-1-cyclohexyl Diazenedicarboxylateâ M. A. Brimble, Electronic Encyclopedia of Reagents for Organic Synthesis [e-EROS], eds L. A. Paquette, D. Crich, P. L. Fuchs and P. Wipf, John Wiley and Sons Inc., 2001. https://doi.org/10.1002/047084289X.rn00005
5. âSynthetic Strategies Towards Pyranonaphthoquinone Antibioticsâ M. A. Brimble, Pure and Applied Chemistry, 2000, 72, 1635-1639. http:// http://doi.org/10.1351/pac200072091635 (IF = 2.8)
4. âSynthetic Strategies Towards Pyranonaphthoquinone Antibioticsâ M. A. Brimble, M. R. Nairn and H. Prabaharan, Tetrahedron, 2000, 56, 1937-1992. http://doi.org/10.1016/S0040-4020(99)01021-2 (IF = 3.0)
3. âSynthetic Studies Towards Natural Products Containing Bis-Spiroacetalsâ M. A. Brimble, Journal of Heterocyclic Chemistry, 1999, 36, 1373-1389. http:// doi.org/10.1002/jhet.5570360603 (IF = 1.2)
2. âSynthesis of Bis-Spiroacetal Ring Systemsâ M. A. Brimble and F. A. Fares, Tetrahedron, 1999, 55, 7661-7706. http://doi.org/10.1016/S0040-4020(99)00387-7 (IF = 3.0)
1. âPyranonaphthoquinone Antibiotics â Isolation, Structure and Biological Activityâ M. A. Brimble, L. J. Duncalf and M. R. Nairn, Natural Product Reports, 1999, 16, 267-281. https://doi.org/10.1039/A804287J (IF = 9.8)
42. M. A. Brimble, G. M. Cook, P. W. R. Harris, D. A. Williamson, A. Davidson and V. Sander
âLipidated Polymyxin Analoguesâ
NZ Patent Application 779028, 2021, filed 12 August 2021
41. J. C. Evans, M. A. Brimble, R. Thota, D. Lomiwes and O. M. Shaw
âAnti-inflammatory Compositions, Methods and Uses Thereofâ
PCT Application, 2021, PCT/NZ2021/050103, filed 2 July 2021
40. A. Podolyan, D. K. Rennison, G. Cook, H. J. Di, K. C. Cameron, M. A. Brimble, S. Ferguson, R. S. Ronimus and V. Carbone
âImprovements in and Relating to Nitrification Inhibitorsâ
NZ Patent Application 774955, 2021, filed 12 April 2021
NZ Patent Application 774851, 2021, filed 9 April 2021
NZ Patent Application 771062, 2020, filed 14 December 2020
NZ Patent Application 765239, 2020, filed 9 June 2020
NZ Patent Application 765211, 2020, filed 8 June 2020
NZ Patent Application 765203, 2020, filed 8 June 2020
NZ Patent Application 764780, 2020, filed 29 May 2020
NZ Patent Application 764783, 2020, filed 26 May 2020
NZ Patent Application 764712, 2020, filed 25 May 2020
39. D. K. Rennison, I. K. Boddy and M. A. Brimble,
âMethanogen Inhibitorsâ
NZ Patent Application 769756, 2020, filed 10 November 2020
38. D. K. Rennison, I. K. Boddy and M. A. Brimble,
âMethanogen Inhibitorsâ
NZ Patent Application 769755, 2020, filed 10 November 2020
37. B. Lin, K. M. Loomes, R. Thota, J. Stephens, J. Evans and M. A. Brimble âAnti-inflammatory Compositions, Methods and Uses Thereofâ PCT Application, 2020, PCT/NZ2020/050065, filed 3 July 2020.
36. W. Greenlee, S. Berezovsky, G. Trainor, M. A. Brimble and G. M. Williams âPeptide Conjugates Incorporating Urea Elements and Their Use as Vaccinesâ U.S. Patent Application No. 16/864,348, 2020, filed May 1, 2020 Claims priority to US Provisional Patent Application No. 62/841,893, 2019, filed May 2, 2019
35. M. A. Brimble, P. W. R. Harris, L. Yule, D. Hay and A. Tufts âPeptide Conjugate Amylin Agonists and Uses Thereofâ PCT International Application PCT/IB2020/054364, 2020, filed 8 May 2020 US Patent Application 34772US01, 2019, filed 8 May 2019
34. L. Stubbing, I. Kavianinia, A. Patterson, J. Smaill, M. Abbattista, P. W. R. Harris and M. A. Brimble âPeptide Compounds, Conjugates thereof, and Uses Thereofâ PCT International Application PCT/IB2019/059597, 2019, filed 8 November 2019 NZ Patent Application 784041, 2018, filed 8 November 2018
33. D. Rennison, M. A. Brimble, G. Cook, S. Ferguson and A. Heikel âQuinoline Sulfonamide Compounds and their use as Antibacterial Agentsâ PCT International Patent WO/2019/125185 A1, 2019, published 27 June 2019 (Application number PCT/NZ2018/050182, 2018, filed 20 December 2018)
32. E. T. Williams, P. W. R. Harris, M. A. Jamaluddin, K. M. Loomes, D. L. Hay, C. Walker and M. A. Brimble âPeptide Conjugate CGRP Receptor Antagonists and Methods of Preparation and Uses Thereofâ US Patent Application 16/762,098, 2020, filed 6 May 2020 PCT International Patent WO/2019/087161 A1, 2019, published 9 May 2019 (Application number PCT/IB2018/058684, 2018, filed 6 November 2018) NZ Patent Application 736960, 2017, filed 6 November 2017
31. M. A. Brimble, P. R. Dunbar, G. M. Williams, D. Verdon âPeptide Conjugates, Conjugation Process and Uses Thereofâ US Patent Application 16/638,185, 2020, filed 2/11/20 Mexican Patent Application, 2020, filed 2/11/20 (Application number PCT/IB2018/056611, 2018, filed 30 August 2018) NZ Patent Application 735008, 2017, filed 30 August 2017
30. M. A. Brimble and J. F. Marshall âTumour-targeting Peptide Variantsâ GB Patent Application GBA201706472, 2017, filed 24 April 2017. PCT/EP2018/060474, 2018, filed 24 April 2018
29. M. A. Brimble, P. R. Dunbar, G. M. Williams, D. Verdon âAmino Acid and Peptide Conjugates and Conjugation Processâ US Patent Application 16/076912, 2019, published 14/2/19 PCT International PCT/IB2017/051054, 2017, filed 24 Feb 2017 National phase in United States, Europe, Canada, Japan, Mexico, Korea, Australia, China, Israel, India, New Zealand, Singapore, Eurasia, Brazil and South Africa (AU Provisional Patent Application 2016900701, 2016, filed 26 Feb 2016) TW Patent Application 106106457, 2017, filed 24 Feb 2017.
28. B. Daniels, G. Prijic, J. Stephens, M. A. Brimble and R. C. Schlothauer PCT International Patent WO2017/099612, 2017, published 15 Jun 2017. âMarker Compounds of Leptospermum Honeys and Methods of Isolation and Assaying Thereofâ NZ Patent 722140, 2016, published 13 Jul 2016. (NZ Provisional Patent Application 715094, 2015, filed 11 Dec 2015)
27. I. A. Summut, J. C. Harrison, R. J. Hewitt, M. I. Read, N. J. Stanley, L. M. Woods, J. T. B. Kueh, M. Jay-Smith, R. A. J. Smith, G. Giles, L. Larsen, D. Rennison, M. A. Brimble and D. S. Larsen âCarbon-Monoxide Releasing Norbornenone Compoundsâ US Patent Application 2018/0346420, 2018, published 6 Dec 2018. NZ Patent 742326; AU Patent 2016364624; US15/779,929; European Patent 16871116.6; Canadian Patent 2016800798926
(Application number PCT/NZ2016/050188, filed 30 Nov 2016) 26. M. A. Brimble, P. R. Dunbar, G. M. Williams and D. Verdon, âAmino Acid and Peptide Conjugates and Uses Thereofâ PCT International Patent WO2016/103192, 2016, published 30 Jun 2016. (Application number PCT/IB2015/059901, filed 22 Dec 2015) US Patent Application 15/535,956, 2018, published 4 Jan 2018
25. B. Naysmith, D. Herman, D. E. Williams, J. Jin, M. A. Brimble and R. Tilley, âPolymers for Coating Nanoparticlesâ PCT International Patent, WO 2015/199555 A1, 2015, published 30 Dec 2015 (Application number PCT/NZ2015/050080, filed 26 Jun 2015)
24. M. A. Brimble, C. Evans, S. Papst and D. E. Williams, âPlatinum Nanoparticle Conjugate for Imaging and Therapyâ UK Patent Application 2014, GB1412968.8, filed 22 Jul 2014.
23. M. A. Brimble and D. P. Furkert âAzo Compoundsâ NZ Provisional Patent Application 622866, 2014, filed 24 Mar 2014.
22. M. A. Brimble, P. R. Dunbar, P. W. R. Harris, G. W. Williams and T. H. Wright, âAmino Acid and Peptide Conjugates and Conjugation Processâ PCT International Patent WO/2014/207708 A2, 2014, published 31 Dec 2014 (Application number PCT/IB2014/062648, filed 27 Jun 2014) Chinese Patent CN 105555756 A, 2016, published 29 Jan 2016. (Application number 201480042833.2, 2014, filed 27 Jun 2014) US Patent Application 14/392,231, 2016, filed 27 Jun 2014. TW Patent Application 103122466, 2014, filed 30 Jun 2014. AU Patent Application 2014300503, 2014, filed 27 Jun 2014. European Patent EP3013789 B1, 2020, published 04 March 2020 (European Patent Application 14818659.6, 2014, filed 27 Jun 2014). HK Patent Application, 2014, filed 27 Jun 2014. JP Patent Application 2016-522936, 2014, filed 27 Jun 2014. âPeptide Conjugates and Conjugation Processâ NZ Provisional Patent Application 612654, 2013, filed 28 June 2013. âAmino Acid and Peptide Conjugates and Conjugation Processâ NZ Patent 626713, 2014, published 27 Jun 2014. NZ Patent 715869, 2016, published 15 Jan 2016.
21. J. Lu, D. Liu, J. Guan, M. A. Brimble, P. W. R. Harris and B. Huang, âApplication of cGP and Derivatives in Preparing Medicine for Inhibiting Tumor Growth and Regenerationâ Chinese Patent CN 103100080 B, 2014, published 18 Jun 2014 (Application number CN201210392352, filed 16 Oct 2012)
20. B. Hopkins, S. Bova, M. Cavali, O. Laita, M. A. Brimble and D. Rennison âPreparation of Norbormide Analoguesâ PCT International Patent WO 2013/133726 A1, 2013, published 12 Sep 2013 (Application number PCT/NZ2013/0000034, filed 11 Mar 2013)
19. G. M. Williams and M. A. Brimble, âSynthetic Polypeptides and Uses Thereofâ PCT International Patent WO 2013/128391 A1, 2013, published 6 Sep 2013 (Application number PCT/IB2013/051583, filed 28 Feb 2013)
18. M. A. Brimble, S. Papst, R. Peltier, R. D. Tilley and D. E. Williams âMetal Nanoparticlesâ US Patent Application 2013/0029920 A1, 2013, published 31 Jan 2013 (Application number 13/561,527, filed 30 Jul 2012)
17. M. A. Brimble, A. F. Noisier and C. S. Harris âMethod for Preparing Amino Acidsâ US Provisional Patent Application 61/729,810, 2012, filed 26 September 2012.
16. M. A. Brimble, S. Papst, R. Peltier, R. D. Tilley and D. E. Williams âIron Nanoparticlesâ NZ Provisional Patent Application 594348, 2011, filed 29 July 2011. NZ Provisional Patent Application 598940, 2012, filed 21 March 2012.
15. B. Hopkins, M. A. Brimble, D. Rennison, S. Bova, M. Cavalli and O. Laita, âRodenticidal Compoundsâ NZ Provisional Patent Application 598698, 2012, filed 9 March 2012. NZ Patent 607967, 2013, filed 31 May 2013.
14. M. J. Bickerdike, M. A. Brimble and E. S. Sirimanne, âCyclic Glycyl-2-Allyl Proline and its Use in Treatment of Peripheral Neuropathyâ PCT International Patent WO 2011/037644 A1, 2011, published 31 Mar 2011. (Application number PCT/US2010/002636, filed 27 Sep 2010) US Patent 2011/0052531 A1, 2011, published 3 Mar 2011 US Patent 8,519,127 B2, 2013, published 27 Aug 2013 (Application number 12/891,280, filed 27 Sep 2010)
13. I. K. Boddy, T. Bogaert, M. A. Brimble and D. Rennison, âAnti-Parasitic Carbazolesâ US Provisional Patent Application 61/468,317, 2011, filed 28 Mar 2011.
12. C. Eason, M. A. Brimble and D. Conole, âVertebrate Pest Controlâ NZ Provisional Patent Application 583496, 2010, filed 22 Feb 2010.
11. P. W. R. Harris, M. A. Brimble and F. Sieg, âSynthetic Analogues of Neural Regeneration Peptidesâ PCT International Patent WO 2009/051844 A1, 2009, published 23 Apr 2009. (Application number PCT/US2008/011951, filed 17 Oct 2008) European Patent EP2212349 B1, 2013, published 07 Aug 2013 (Application number 08840727.5, filed 17 Oct 2008)
10. M. A. Brimble, P. W. R. Harris and F. Sieg âAnalogs of Glycyl-Prolyl-Glutamateâ US Patent 2008/0145335 A1, 2008, published 19 Jun 2008 (Application number 11/986,518, filed 20 Nov 2007)
9. P. D. Gluckman, J. Guan, M. A. Woodnorth and M. A. Brimble, âCognitive Enhancement and Cognitive Therapy Using Glycyl-L-2-Methylprolyl-L-Glutamic Acidâ US Patent 8,637,567 B2, 2014, published 28 Jan 2014. (Application number 12/903,844, filed 13 Oct 2010)
8. P. D. Gluckman, G. B. Thomas, J. Guan, M. Dragunow, A. K. Anand, F. Sieg and M. A. Brimble, âEffects of Glycyl-2 Methyl Prolyl Glutamate on Neurodegenerationâ US Patent 7,605,177 B2, 2009, published 20 Oct 2009. (Application number 11/314,424, filed 20 Dec 2005)
7. M. A. Brimble and J. Guan, âCyclic G-2-Allylproline in Treatment of Parkinson’s Diseaseâ US Patent 7,776,876 B2, 2010, published 17 Aug 2010 (Application number 11/399,974, filed 7 Apr 2006)
6. F. Sieg, M. A. Brimble and V. J. Muir, âNeural Regeneration Peptides and Methods for Their Useâ PCT International Patent WO 2006/121926 A2, 2006, published 16 Nov 2006 (Application number PCT/US2006/017534, filed 5 May 2006) European Patent EP1888635 A2, 2008, published 20 Feb 2008 (Application number EP20060752652, filed 5 May 2006) âNeural Regeneration Peptides and Formulations Thereofâ US Patent 8,138,304 B2, 2012, published 20 Mar 2012 (Application number 11/919,952, filed 5 May 2006.
5. M. A. Brimble, P. W. R. Harris and F. Sieg, âAnalogs of Glycyl-Prolyl-Glutamateâ PCT International Patent WO 2006/127702 A2, 2006, published 30 Nov 2006 (Application number PCT/US2006/019909, filed 23 May 2006) European Patent EP1888618 A4, 2009, published 15 Jul 2009 (Application number EP20060770950, filed 23 May 2006)
4. P. D. Gluckman, M. A. Brimble, D. Wilson, F. C. Tortella, A. J. Williams, X.-C. M. Lu, J. A. Hartings and D. Gryder, âTreatment of Non-Convulsive Seizures in Brain Injury Using G-2-Methyl-Prolyl Glutamateâ US Patent 7,714,020 B2, 2010, published 11 May 2010 (Application number 11/398,032, filed 4 Apr 2006)
3. M. A. Brimble, J. Guan and F. Sieg, âNeuroprotective Bicyclic Compounds and Methods for Their Useâ PCT International Patent WO 2005/023815 A3, 2005, published 21 Jul 2005 (Application number PCT/US2004/028308, filed 31 Aug 2004) US Patent 8,067,425 B2, 2011, published 29 Nov 2011 (Application number 10/570,395, filed 31 Aug 2004) âNeuroprotective Bicyclic Compounds and Pharmaceutical Compositions Containing Themâ European Patent EP1664050 A2, 2006, published 7 Jun 2006 (Application number EP20040782733, filed 31 Aug 2004)
2. P. W. R. Harris and M. A. Brimble, âNeuroprotective Macrocylic Compounds and Methods for Their Useâ PCT International Patent WO 2004/084809 A3, 2005, published 30 Jun 2005 (Application number PCT/US2004/008108, filed 16 Mar 2004) European Patent EP1648873 A4, 2008, published 25 Jun 2008 (Application number EP20040757761, filed 16 Mar 2004)
1. N. A. Abood and M. A. Brimble, âGPE Analogs and Peptidomimeticsâ PCT International Patent WO 2002094856 A3, 2003, published 15 May 2003 (Application number PCT/US2002/016361, filed 24 May 2002) US Patent 7,041,314 B2, 2006, published 9 May 2006. (Application number 10/155,864, filed 24 May 2002) Australian Patent 2002/303856 A1, 2002, filed 3 Dec 2002