Issue 9, 1992
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

A chemoenzymatic synthesis of enantiomerically pure (R)- and (S)-2-methyldecan-1-ol

Patrizia Ferraboschi,   Paride Grisenti,   Ada Manzocchi  and  Enzo Santaniello  

Abstract

(R)- and (S)-2-methyldecan-1-ol 3a has been prepared in >98% enantiomeric excess (ee) by transesterification with vinyl acetate in chloroform in the presence of Pseudomonas fluorescens lipase. Oxidation of the alcohol 3a affords nearly optically pure 2-methyldecanoic acid 3b

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Article information

DOI
https://doi.org/10.1039/P19920001159
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 1159-1161

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A chemoenzymatic synthesis of enantiomerically pure (R)- and (S)-2-methyldecan-1-ol

P. Ferraboschi, P. Grisenti, A. Manzocchi and E. Santaniello, J. Chem. Soc., Perkin Trans. 1, 1992, 1159 DOI: 10.1039/P19920001159

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