Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/5767
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dc.contributor.authorSilva, M. Manuel Cruz-
dc.contributor.authorRiva, Sergio-
dc.contributor.authorMelo, M. Luísa Sá e-
dc.date.accessioned2008-09-26T17:41:24Z-
dc.date.available2008-09-26T17:41:24Z-
dc.date.issued2004en_US
dc.identifier.citationTetrahedron: Asymmetry. 15:7 (2004) 1173-1179en_US
dc.identifier.urihttps://hdl.handle.net/10316/5767-
dc.description.abstractStereoisomerically pure 3[beta]-hydroxy-5,6-epoxysteroids were obtained by combining selective chemical methods for [alpha]- and [beta]-epoxidation of [Delta]5-unsaturated steroids with enzymatic stereoselective esterification of the 3[beta]-hydroxyl group. 5[beta],6[beta]-Epoxy-3[beta]-hydroxysteroids were efficiently acylated by Novozym 435 and lipase AK, whereas 5[alpha],6[alpha]-epoxy-3[beta]-hydroxysteroids were good substrates for Candida rugosa lipase. Mild enzymatic deacylation of the 3[beta]-acetoxy group in the presence of the epoxy functionality was also accomplished by C. rugosa lipase-mediated hydrolysis.en_US
dc.description.urihttp://www.sciencedirect.com/science/article/B6THT-4BY3V2F-3/1/14f2ed3d64a39572337a2fd7eda27712en_US
dc.format.mimetypeaplication/PDFen
dc.language.isoengeng
dc.rightsopenAccesseng
dc.titleHighly selective lipase-mediated discrimination of diastereomeric 5,6-epoxysteroidsen_US
dc.typearticleen_US
dc.identifier.doi10.1016/j.tetasy.2004.02.010-
item.openairetypearticle-
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-1938-4150-
Appears in Collections:FFUC- Artigos em Revistas Internacionais
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