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dc.contributor.authorHoffmann, Joseph J.-
dc.contributor.authorFraga, Braulio M.-
dc.date.accessioned2010-03-03T08:56:18Z-
dc.date.available2010-03-03T08:56:18Z-
dc.date.issued1993-
dc.identifier.citationPhytochemistry 33(4): pp. 827-830 (1993)en_US
dc.identifier.issn0031-9422-
dc.identifier.urihttp://hdl.handle.net/10261/21851-
dc.description.abstractWhen 17-acetoxy-kolavenol acetate was subjected to biotransformation with Mucor plumbeus, the substrate was deacylated and converted into 17,19-dihdroxy-kolavenol 3,4,17-trihydroxy-3a,4B-dihydro-kolavenol, and an isomeric mixture of 13,17,19-trihydroxy-clerod-14,15-ene. The three compounds were identified as their acetate derivatives.en_US
dc.description.sponsorshipThe authors are grateful to Kennethj Tomlinson and Lou Hutter for the bulk work-up of Vanclevea to generate sufficient quantities of Ia. This work was done in part during Dr. Hoffmann's sabbatical leave at the Institute and the thanks the Institute for its support.en_US
dc.format.extent128140 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsopenAccessen_US
dc.subjectMucor plumbeusen_US
dc.subjectBiotransformationsen_US
dc.subjectDiterpenesen_US
dc.subjectClerodanesen_US
dc.subjectKolavene derivativesen_US
dc.titleMicrobial transformation of diterpenes: hidroxylation of 17-acetoxy-kolavenol acetate by Mucor plumbeusen_US
dc.typeartículoen_US
dc.description.peerreviewedPeer revieweden_US
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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