Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+/-)-3-hydroxy-4-chromanone by Trichosporon cutaneum

dc.creatorLunardi, I
dc.creatorConceicao, GJA
dc.creatorMoran, PJS
dc.creatorRodrigues, JAR
dc.date2005
dc.dateAUG 1
dc.date2014-11-18T10:49:36Z
dc.date2015-11-26T16:54:03Z
dc.date2014-11-18T10:49:36Z
dc.date2015-11-26T16:54:03Z
dc.date.accessioned2018-03-28T23:41:17Z
dc.date.available2018-03-28T23:41:17Z
dc.identifierTetrahedron-asymmetry. Pergamon-elsevier Science Ltd, v. 16, n. 15, n. 2515, n. 2519, 2005.
dc.identifier0957-4166
dc.identifierWOS:000234625700001
dc.identifier10.1016/j.tetasy.2005.06.020
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/68423
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/68423
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/68423
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1276749
dc.descriptionDeracernization of (+/-)-3-hydroxy-4-chrornan one 2 through stercoselective bioreduction to the corresponding (3R,4S)-3,4-chromanediol 3, with good to excellent enantiomeric excesses (LIP to 99%). mediated by resting cells of the yeast Trichosporon cutaneum CCT 1903, is reported. In addition, 3-hydroxychronione (7) was obtained as a secondary product. (c) 2005 Elsevier Ltd. All rights reserved.
dc.description16
dc.description15
dc.description2515
dc.description2519
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationTetrahedron-asymmetry
dc.relationTetrahedron: Asymmetry
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectProtease Inhibitors
dc.titleHighly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+/-)-3-hydroxy-4-chromanone by Trichosporon cutaneum
dc.typeArtículos de revistas


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