Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of Brazilian micro-organisms
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2008
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Resumo |
The use of whole cells of micro-organisms to bring about the biotransformation of an organic compound offers a number of advantages, but problems caused by enzymatic Promiscuity may be encountered upon With Substrates hearing more than one functional group. A one-pot screening method, in which whole fungal cells were incubated with a Mixture of 4-rnethylcyclohexanone I and phenyl methyl Sulfide 2, has been employed to determine the chemoselectivity of various biocatalysts. The hyphomycetes, Aspergillus terreus CCT 3320 and A. terreus URM 3571, catalysed the oxidation of 2 accompanied by the reduction of I to 4-methylcyclohexanol 1a and, for strain A. terreus CCT 3320, the Baeyer-Villiger oxidation of 1. The Basidomycetes, Trametes versicolor CCB 202, Pycnoporus sanguineus CCB 501 and Trichaptum byssogenum CCB 203, catalysed the oxidation of 2 and the reduction 1, but no Baeyer-Villiger reaction products were detected. In contrast. Trametes rigida CCB 285 catalysed the biotransformation of 1 to 1a, exclusively, in the absence of any detectable Sulfide oxidation reactions. The chemoselective reduction Of (+/-)-2-(phenylthio)cyclohexanone 3 by T. rigida CCB 285 afforded exclusively the (+)-cis-(1R,2S) and (+)-trans-(1S,2S) diastereoisomers of 2-(phenylthio)cyclohexan-1-ol 3a in moderate yields (13% and 27%, respectively) and high enantiomeric excesses (>98%). Chemoselective screening for the reduction of a ketone and/or the oxidation Of a Sulfide group in one pot by whole cells of micro-organisms represents an attractive technique with applications in the development of synthesis of complex molecule hearing different functional groups. (C) 2008 Published by Elsevier Ltd. Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) FAPESP[05/52941-7] Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) FAPESP[03/04189-9] Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) CNPq[472663/2004-6] |
Identificador |
TETRAHEDRON-ASYMMETRY, v.19, n.20, p.2385-2389, 2008 0957-4166 http://producao.usp.br/handle/BDPI/31263 10.1016/j.tetasy.2008.10.003 |
Idioma(s) |
eng |
Publicador |
PERGAMON-ELSEVIER SCIENCE LTD |
Relação |
Tetrahedron-asymmetry |
Direitos |
restrictedAccess Copyright PERGAMON-ELSEVIER SCIENCE LTD |
Palavras-Chave | #ASPERGILLUS-TERREUS #ENZYME PROMISCUITY #CARBONYL-COMPOUNDS #RHIZOPUS-ORYZAE #CYCLIC-KETONES #LIPASE #BIOTRANSFORMATION #MONOOXYGENASES #SULFOXIDES #RESOLUTION #Chemistry, Inorganic & Nuclear #Chemistry, Organic #Chemistry, Physical |
Tipo |
article original article publishedVersion |