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

Galina Dmitrievna Gamalevich 1
Galina Dmitrievna Gamalevich
Edward Prokof'evich Serebryakov 1
Edward Prokof'evich Serebryakov
Alexei Leonidovich Vlasyuk 2
Alexei Leonidovich Vlasyuk
Published 1998-02-28
CommunicationVolume 8, Issue 1, 8-9
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Gamalevich G. D., Serebryakov E. P., Vlasyuk A. L. Lipase-mediated stereodivergent synthesis of both enantiomers of 4-(2,6-dimethylheptyl)benzoic acid // Mendeleev Communications. 1998. Vol. 8. No. 1. pp. 8-9.
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Gamalevich G. D., Serebryakov E. P., Vlasyuk A. L. Lipase-mediated stereodivergent synthesis of both enantiomers of 4-(2,6-dimethylheptyl)benzoic acid // Mendeleev Communications. 1998. Vol. 8. No. 1. pp. 8-9.
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TY - JOUR
DO - 10.1070/MC1998v008n01ABEH000890
UR - https://mendcomm.colab.ws/publications/10.1070/MC1998v008n01ABEH000890
TI - Lipase-mediated stereodivergent synthesis of both enantiomers of 4-(2,6-dimethylheptyl)benzoic acid
T2 - Mendeleev Communications
AU - Gamalevich, Galina Dmitrievna
AU - Serebryakov, Edward Prokof'evich
AU - Vlasyuk, Alexei Leonidovich
PY - 1998
DA - 1998/02/28
PB - Mendeleev Communications
SP - 8-9
IS - 1
VL - 8
ER -
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@article{1998_Gamalevich,
author = {Galina Dmitrievna Gamalevich and Edward Prokof'evich Serebryakov and Alexei Leonidovich Vlasyuk},
title = {Lipase-mediated stereodivergent synthesis of both enantiomers of 4-(2,6-dimethylheptyl)benzoic acid},
journal = {Mendeleev Communications},
year = {1998},
volume = {8},
publisher = {Mendeleev Communications},
month = {Feb},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1998v008n01ABEH000890},
number = {1},
pages = {8--9},
doi = {10.1070/MC1998v008n01ABEH000890}
}
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Gamalevich, Galina Dmitrievna, et al. “Lipase-mediated stereodivergent synthesis of both enantiomers of 4-(2,6-dimethylheptyl)benzoic acid.” Mendeleev Communications, vol. 8, no. 1, Feb. 1998, pp. 8-9. https://mendcomm.colab.ws/publications/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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