Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/5756
DC FieldValueLanguage
dc.contributor.authorSilva, M. Manuel Cruz-
dc.contributor.authorRiva, Sergio-
dc.contributor.authorMelo, M. Luísa Sá e-
dc.date.accessioned2008-09-26T17:41:12Z-
dc.date.available2008-09-26T17:41:12Z-
dc.date.issued2005en_US
dc.identifier.citationTetrahedron. 61:12 (2005) 3065-3073en_US
dc.identifier.urihttps://hdl.handle.net/10316/5756-
dc.description.abstractMonoacylated derivatives of a complete set of 2,3- and 3,4-vicinal diols of steroids were prepared by regioselective lipase-catalysed transesterification reactions. The enzymes displayed different selectivities towards the vicinal diols depending on the configuration of the hydroxyl groups.en_US
dc.description.urihttp://www.sciencedirect.com/science/article/B6THR-4FGX84H-2/1/c23744db4c590d02acf7c82018be5720en_US
dc.format.mimetypeaplication/PDFen
dc.language.isoengeng
dc.rightsopenAccesseng
dc.subjectLipasesen_US
dc.subjectSteroidsen_US
dc.subjectRegioselectivityen_US
dc.subjectEnzymatic esterificationen_US
dc.titleRegioselective enzymatic acylation of vicinal diols of steroidsen_US
dc.typearticleen_US
dc.identifier.doi10.1016/j.tet.2005.01.104-
item.languageiso639-1en-
item.openairetypearticle-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
item.cerifentitytypePublications-
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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