Issue 4, 1992

Biotransformations using clostridia: stereospecific reductions of a β-keto ester

Abstract

The reduction of methyle 4-(4-chlorophenylthio)-3-oxobutanoate 1 by clostridia has been studied. Clostridium pasteurianum ATCC 6013, C. tyrobutyricum DSM 1460 and C. kluyveri NCIB 10680 gave the D-(3S) reduction product 2, whereas C. kluyveri DSM 555 gave the L-(3R) reduction product 3. The products could be obtained in higher optical purities than by yeast reductions.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 491-493

Biotransformations using clostridia: stereospecific reductions of a β-keto ester

M. Christen, D. H. G. Crout, R. A. Holt, J. G. Morris and H. Simon, J. Chem. Soc., Perkin Trans. 1, 1992, 491 DOI: 10.1039/P19920000491

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