S
Sharon Chow
Researcher at University of Queensland
Publications - 39
Citations - 489
Sharon Chow is an academic researcher from University of Queensland. The author has contributed to research in topics: Pimelea & Catalysis. The author has an hindex of 12, co-authored 37 publications receiving 412 citations. Previous affiliations of Sharon Chow include Animal Research Institute.
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Hydrolytic kinetic resolution of terminal mono- and bis-epoxides in the synthesis of insect pheromones: routes to (−)-(R)- and (+)-(S)-10-methyldodecyl acetate, (−)-(R)-10-methyl-2-tridecanone, (−)-(R)-(Z)-undec-6-en-2-ol (Nostrenol), (−)-(1R,7R)-1,7-dimethylnonyl propanoate, (−)-(6R,12R)-6,12-dimethylpentadecan-2-one, (−)-(2S,11S)-2,11-diacetoxytridecane and (+)-(2S,12S)-2,12-diacetoxytridecane
Sharon Chow,William Kitching +1 more
TL;DR: In this article, the authors used hydrolytic kinetic resolution (HKR) of functionalised epoxides using (salen)Co(OAc) complexes to obtain enantiomerically enriched epoxide and diols which have been transformed into important insect sex pheromones.
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Daphnane- and Tigliane-Type Diterpenoid Esters and Orthoesters from Pimelea elongata.
TL;DR: Eight new tigliane- and daphnane-type diterpenes were found in Pimelea elongata, and the structures and relative configurations of the new compounds were determined by 1D and 2D NMR spectroscopic studies in combination with MS analyses.
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Determining a synthetic approach to pierisformaside C.
TL;DR: An efficient route detailing the construction of the central core of pierisformaside C, the first grayanane-type diterpene to possess three central double bonds, is reported.
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Synthesis of the Sponge-Derived Plakortone Series of Bioactive Compounds
Patricia Y. Hayes,Sharon Chow,Fredrik Rahm,Paul V. Bernhardt,James J. De Voss,William Kitching +5 more
TL;DR: The Caribbean sponges of the genus Plakortis, P. halichondrioides, and P. simplex have provided a series of biologically active furanolactones-the plakortones A-D from the former sponge and B-F from the latter, which settle constitutional and stereochemical features in this group of secondary metabolites.
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Novel cuticular hydrocarbons from the cane beetle Antitrogus parvulus--4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes-unprecedented anti-anti-anti-stereochemistry in the 4,6,8,10-methyltetrad.
Sharon Chow,Mary T. Fletcher,Lynette K. Lambert,Oliver P. Gallagher,Christopher J. Moore,Bronwen W. Cribb,Peter G. Allsopp,William Kitching +7 more
TL;DR: Capillary gas chromatography, mass spectrometry, and high resolution 13C NMR spectroscopy confirmed 1 as either 84a or 84b and 2 as either 15a or 15b and the novelty of these structures and their relative stereochemistry is briefly related to polyketide assembly.