G. D. Gamalevich, E. P. Serebryakov, A. L. Vlasyuk, “Lipase-mediated stereodivergent synthesis of both enantiomers of 4-(2,6-dimethylheptyl)benzoic acid”, Mendeleev Commun., 8:1 (1998), 8

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Mendeleev Communications, 1998, Volume 8, Issue 1, Pages 8–9
DOI: https://doi.org/10.1070/MC1998v008n01ABEH000890 (Mi mendc4628)

This article is cited in 4 scientific papers (total in 4 papers)

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

G. D. Gamalevich^a, E. P. Serebryakov^a, A. L. Vlasyuk^b

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b Higher Chemical College of the Russian Academy of Sciences, D.I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation

Full-text PDF (93 kB) Citations (4)

DOI: https://doi.org/10.1070/MC1998v008n01ABEH000890

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/Et₂O acylating system, have been converted in four steps into the (R)- and (S)-enantiomers of the title acid, respectively.

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Document Type: Article

Language: English

Citation: G. D. Gamalevich, E. P. Serebryakov, A. L. Vlasyuk, “Lipase-mediated stereodivergent synthesis of both enantiomers of 4-(2,6-dimethylheptyl)benzoic acid”, Mendeleev Commun., 8:1 (1998), 8–9

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This publication is cited in the following 4 articles:

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