Please use this identifier to cite or link to this item:
https://hdl.handle.net/10316/5756
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Silva, M. Manuel Cruz | - |
dc.contributor.author | Riva, Sergio | - |
dc.contributor.author | Melo, M. Luísa Sá e | - |
dc.date.accessioned | 2008-09-26T17:41:12Z | - |
dc.date.available | 2008-09-26T17:41:12Z | - |
dc.date.issued | 2005 | en_US |
dc.identifier.citation | Tetrahedron. 61:12 (2005) 3065-3073 | en_US |
dc.identifier.uri | https://hdl.handle.net/10316/5756 | - |
dc.description.abstract | Monoacylated 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.uri | http://www.sciencedirect.com/science/article/B6THR-4FGX84H-2/1/c23744db4c590d02acf7c82018be5720 | en_US |
dc.format.mimetype | aplication/PDF | en |
dc.language.iso | eng | eng |
dc.rights | openAccess | eng |
dc.subject | Lipases | en_US |
dc.subject | Steroids | en_US |
dc.subject | Regioselectivity | en_US |
dc.subject | Enzymatic esterification | en_US |
dc.title | Regioselective enzymatic acylation of vicinal diols of steroids | en_US |
dc.type | article | en_US |
dc.identifier.doi | 10.1016/j.tet.2005.01.104 | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | article | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | open | - |
item.fulltext | Com Texto completo | - |
item.languageiso639-1 | en | - |
crisitem.author.researchunit | CNC - Center for Neuroscience and Cell Biology | - |
crisitem.author.orcid | 0000-0002-1938-4150 | - |
Appears in Collections: | FFUC- Artigos em Revistas Internacionais |
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File | Description | Size | Format | |
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file556817ff2179478a9ae1aba4d2ddeb53.pdf | 249.96 kB | Adobe PDF | View/Open |
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