Bioreduction of alpha-haloacetophenones by Rhodotorula glutinis and Geotrichum candidum

dc.creatorFardelone, LC
dc.creatorRodrigues, JAR
dc.creatorMoran, PJS
dc.date2003
dc.date2014-11-15T23:17:20Z
dc.date2015-11-26T17:22:30Z
dc.date2014-11-15T23:17:20Z
dc.date2015-11-26T17:22:30Z
dc.date.accessioned2018-03-29T00:09:57Z
dc.date.available2018-03-29T00:09:57Z
dc.identifierArkivoc. Arkat Usa Inc, n. 404, n. 410, 2003.
dc.identifier1551-7012
dc.identifierWOS:000220556500038
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/55657
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/55657
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/55657
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1283621
dc.descriptionEnantioselective reductions with enantiocomplementarity of alpha-haloacetophenones by Rhodotorula glutinis CCT 2182 and Geotrichum candidum CCT 1205 afforded the corresponding (R)- and (S)-halohydrins (halo = Cl, Br and I), respectively, in high chemical yields (89-99%) and enantiomeric excesses (92-99%). These halohydrins are potential chiral building blocks for the stereoselective syntheses of valuable compounds.
dc.description10
dc.description404
dc.description410
dc.languageen
dc.publisherArkat Usa Inc
dc.publisherGainesville
dc.publisherEUA
dc.relationArkivoc
dc.relationArkivoc
dc.rightsaberto
dc.sourceWeb of Science
dc.subjectbioreduction
dc.subjectalpha-haloacetophenones
dc.subjectRhodotorula glutinis
dc.subjectGeotrichum candidum
dc.subjectBakers-yeast Reduction
dc.subjectHydride Transfer
dc.subjectKetones
dc.titleBioreduction of alpha-haloacetophenones by Rhodotorula glutinis and Geotrichum candidum
dc.typeArtículos de revistas


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