Microbial hydroxylation/functionalization of terpenoid synthons derived from communic acids

Abstract : Incubation of a communic acid-derived synthon with Cunninghamella elegans quantitatively affords 1ß, 3ß- and 7ß-monohydroxylated derivatives. (C) 2000 Elsevier Science Ltd.
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Submitted on : Tuesday, March 11, 2014 - 1:30:38 PM
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Gérard Aranda, R. Azerad, M. Maurs, G. Bertho, D. Jiménez-González, et al.. Microbial hydroxylation/functionalization of terpenoid synthons derived from communic acids. Phytochemistry, Elsevier, 2000, 54 (1), pp.23-27. ⟨10.1016/s0031-9422(00)00032-7⟩. ⟨hal-00954903⟩

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