Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/94502
Type: Artigo de evento
Title: Baker's Yeast Mediated Asymmetric Reduction Of Cinnamaldehyde Derivatives
Author: Fardelone L.C.
Augusto J.
Rodrigues R.
Moran P.J.S.
Abstract: The enantioselective reduction of cinnamaldehyde derivatives is an attractive strategy to prepare various optically active multifunctional molecules that can be used as chiral building blocks for the synthesis of some HIV-protease inhibitors. The asymmetric reduction with pH adjusted to 5.5 of α-substituted-cinnamaldehydes (Br, N 3) mediated by baker's yeast (Saccharomyces cerevisiae) yielded α-substituted-3-phenyl-1-propanol in excellent enantiomeric excesses and yields. © 2004 Elsevier B.V. All rights reserved.
Editor: 
Rights: fechado
Identifier DOI: 10.1016/j.molcatb.2003.10.017
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-2442520385&partnerID=40&md5=4bb555b5497f5f81ea440c492bf2c0c0
Date Issue: 2004
Appears in Collections:Unicamp - Artigos e Outros Documentos

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