Аннотация:
(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.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4628
https://www.mathnet.ru/rus/mendc/v8/i1/p8
Эта публикация цитируется в следующих 4 статьяx:
G. D. Gamalevich, A. L. Vlasyuk, É. P. Serebryakov, “Synthesis of the Racemate and Both Enantiomers of Biologically Active 4-(2,6-Dimethylheptyl)Benzoic Acid and Their Effect on Cholesterol Accumulation in Aorta Cells”, Pharm Chem J, 49:2 (2015), 73
E. P. Serebryakov, G. M. Zhdankina, G. V. Kryshtal', A. N. Orekhov, V. V. Tertov, L. V. Filatova, “Antiatherosclerotic properties of 4-(2,6-dimethylheptyl)-and 4-(2,6,10-trimethylundecyl)benzoic acids and their amides”, Pharm Chem J, 40:12 (2006), 639
G. D. Gamalevich, A. L. Vlasyuk, V. A. Voblikova, E. P. Serebryakov, “Absolute configuration and anti-hypercholesterolemic activity of (+)- and (-)-4-(2,6-dimethylheptyl)benzoic acids”, Russ Chem Bull, 49:7 (2000), 1313
G. D. GAMALEVICH, E. P. SEREBRYAKOV, A. L. VLASYUK, “ChemInform Abstract: Lipase‐Mediated Stereodivergent Synthesis of Both Enantiomers of 4‐(2,6‐Dimethylheptyl)benzoic Acid.”, ChemInform, 29:30 (1998)
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