Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/102394
Type: Artigo de periódico
Title: Bioreduction Of α-haloacetophenones By Rhodotorula Glutinis Andgeotrichum Candidum
Author: Fardelone L.C.
Rodrigues J.A.R.
Moran P.J.S.
Abstract: Enantioselective reductions with enantiocomplementarity of α-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.
Editor: 
Rights: fechado
Identifier DOI: 
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-3242741889&partnerID=40&md5=2e413006f3775cd91af5eb3ab7ff5def
Date Issue: 2003
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
2-s2.0-3242741889.pdf91.82 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.