Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/328048
Type: Artigo
Title: Bioreduction Of Alpha-acetoxymethyl Enones: Proposal For An S(n)2 ' Mechanism Catalyzed By Enereductase
Author: Paula
Bruno R. S.; Zampieri
Davila; Rodrigues
J. Augusto R.; Morana
Paulo J. S.
Abstract: (Z)-3-Acetoxymethyl-4-R-3-buten-2-ones (R= aryl, alkyl) and (Z)-3-methyl-4-R-3-buten-2-ones (R= aryl) were synthesized and submitted to reduction by the yeast Saccharomyces cerevisiae producing the (R)-and (S)-4-R-3-methybutan-2-ones, respectively. This stereochemistry control strategy was applied in the syntheses of (R)-and (S)-Tropional U with moderate to high enantiomeric excesses. Other (Z)-3-acyloxymethyl-4-phenyl-3-buten-2-ones showed similar behavior to the (Z)-3-acetoxymethyl counterpart, and the acylated Morita-Baylis-Hillman adduct 1-acetoxy-2-methylene-1-phenylbutan-3-one produced a mixture of products, with and without the acetoxy group, via three different reaction path-ways. In addition to experiments employing whole cells, those in which isolated enereductases were used suggested that the main pathway through which the loss of the acetoxy group occurs during the biocatalytic cascade is an S(N)2'-type reaction, rather than formal hydrogen addition followed by acetic acid elimination. Finally, related ethyl enones were reduced enantioselectively by the yeast Candida albicans, producing both (R)-and (S)-reduction products, depending on the presence of the acetoxy group in the starting material.
Subject: Biotransformation
Enantioselectivity
Enones
Enzyme Catalysis
Editor: Wiley-V C H Verlag Gmbh
Weinhem
Citation: Advanced Synthesis & Catalysis. Wiley-v C H Verlag Gmbh, v. 358, p. 3555 - 3571, 2016.
Rights: fechado
Identifier DOI: 10.1002/adsc.201600601
Address: http://www.bv.fapesp.br/pt/publicacao/124618/bioreduction-of-alpha-acetoxymethyl-enones-proposal-for-an/
Date Issue: 2016
Appears in Collections:Unicamp - Artigos e Outros Documentos

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