Homochiral (1S,2R)-1,2-indandiol from asymmetric reduction of 1,2-indanedione by resting cells of the yeast Trichosporon cutaneum

dc.creatorConceicao, GJA
dc.creatorMoran, PJS
dc.creatorRodrigues, JAR
dc.date2003
dc.dateAUG 15
dc.date2014-11-15T16:16:56Z
dc.date2015-11-26T16:11:59Z
dc.date2014-11-15T16:16:56Z
dc.date2015-11-26T16:11:59Z
dc.date.accessioned2018-03-28T23:00:29Z
dc.date.available2018-03-28T23:00:29Z
dc.identifierTetrahedron-asymmetry. Pergamon-elsevier Science Ltd, v. 14, n. 16, n. 2327, n. 2330, 2003.
dc.identifier0957-4166
dc.identifierWOS:000184857200002
dc.identifier10.1016/S0957-4166(03)00487-7
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/69610
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/69610
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/69610
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1267225
dc.descriptionA concise highly diastereo- and enantioselective preparation of homochiral (1S,2R)-1,2-indandiol 1 (75% yield, >99% e.e.) by asymmetric reduction of 1,2-indanedione 5 mediated by fresh resting cells of Trichosporon cutaneum CCT 1903 is reported. (C) 2003 Elsevier Ltd. All rights reserved.
dc.description14
dc.description16
dc.description2327
dc.description2330
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.titleHomochiral (1S,2R)-1,2-indandiol from asymmetric reduction of 1,2-indanedione by resting cells of the yeast Trichosporon cutaneum
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución