Margaret A. Brimble
University of Auckland
School of Chemical Sciences
23 Symonds Street
Auckland 1043
New Zealand
Name/email consistency: high
- The Kulinkovich hydroxycyclopropanation reaction in natural product synthesis. Haym, I., Brimble, M.A. Org. Biomol. Chem. (2012)
- Enantioselective synthesis of C-linked spiroacetal-triazoles as privileged natural product-like scaffolds. Kueh, J.T., Choi, K.W., Brimble, M.A. Org. Biomol. Chem. (2012)
- Enantioselective synthesis of pyranonaphthoquinone antibiotics using a CBS reduction/cross-metathesis/oxa-Michael strategy. Hume, P.A., Sperry, J., Brimble, M.A. Org. Biomol. Chem. (2011)
- Synthesis of fluorescein-labelled O-mannosylated peptides as components for synthetic vaccines: comparison of two synthetic strategies. Brimble, M.A., Kowalczyk, R., Harris, P.W., Dunbar, P.R., Muir, V.J. Org. Biomol. Chem. (2008)
- Synthesis and assignment of the absolute configuration of the anti-Helicobacter pylori agents CJ-12,954 and CJ-13,014. Brimble, M.A., Bryant, C.J. Org. Biomol. Chem. (2007)
- Synthesis of the spiroacetal-containing anti-Helicobacter pylori agents CJ-12,954 and CJ-13,014. Brimble, M.A., Bryant, C.J. Chem. Commun. (Camb.) (2006)
- A review of agents patented for their neuroprotective properties. Brimble, M.A., Levi, M.S. Recent. Patents. Cns. Drug. Discovery (2006)
- Synthesis and pharmacological evaluation of side chain modified glutamic acid analogues of the neuroprotective agent glycyl-L-prolyl-L-glutamic acid (GPE). Brimble, M.A., Trotter, N.S., Harris, P.W., Sieg, F. Bioorg. Med. Chem. (2005)
- Synthesis 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 epoxide. Brimble, M.A., Furkert, D.P. Org. Biomol. Chem. (2004)
- Radical oxidative cyclization of spiroacetals to bis-spiroacetals: an overview. Brimble, M.A. Molecules (2004)
