Issue 1, 1998
From the journal:

Mendeleev Communications

Lipase-mediated stereodivergent synthesis of both enantiomers of 4-(2,6-dimethylheptyl)benzoic acid

Galina D. Gamalevich,   Edward P. Serebryakov  and  Alexei L. Vlasyuk  

Abstract

(S)- and (R)-Enantiomers of methyl 4-(3-hydroxy-2-methylpropyl)benzoate, obtained by enzymatic kinetic resolution of the related racemic arene(tricarbonyl)chromium complex in the vinyl acetate-PPL/;Et 2 O acylating system, have been converted in four steps into the (R)- and (S)-enantiomers of the title acid, respectively.

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Article information

DOI
https://doi.org/10.1070/MC1998v008n01ABEH000890
Article type
Paper

Mendeleev Commun., 1998,8, 8-9

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Lipase-mediated stereodivergent synthesis of both enantiomers of 4-(2,6-dimethylheptyl)benzoic acid

G. D. Gamalevich, E. P. Serebryakov and A. L. Vlasyuk, Mendeleev Commun., 1998, 8, 8 DOI: 10.1070/MC1998v008n01ABEH000890

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