Аннотация:
A kinetic resolution of racemic (cyclohexyl)(geranyl)acetic acid, the active ingredient of wound-curing medication Cygerol, to (S)- and (R)-enantiomers was achieved by diastereoselective esterification with (S)- or (R)-BINOL.
Образец цитирования:
S. G. Zlotin, G. V. Kryshtal', G. M. Zhdankina, A. A. Sukhanova, A. S. Kucherenko, B. B. Smirnov, V. A. Tartakovsky, “Kinetic resolution of racemic (cyclohexyl)(geranyl)acetic acid”, Mendeleev Commun., 24:5 (2014), 257–259
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2543
https://www.mathnet.ru/rus/mendc/v24/i5/p257
Эта публикация цитируется в следующих 4 статьяx:
Mohamed Touaibia, Chahrazed Boutekedjiret, Sandrine Perino, Farid Chemat, Green Chemistry and Sustainable Technology, Plant Based “Green Chemistry 2.0”, 2019, 171
Anna A. Sukhanova, Ilya A. Puchkin, Andrei A. Vasil'ev, Sergei G. Zlotin, “Synthesis and stereochemical assignment of geraniol- and nerol-derived Cygerol enantiomers”, Tetrahedron: Asymmetry, 28:12 (2017), 1834
Galina V. Kryshtal, Galina M. Zhdankina, Nikolai V. Ignat'ev, Michael Schulte, Sergei G. Zlotin, “The orthoester Johnson–Claisen rearrangement of allylic terpenols in the presence of acidic ionic liquid”, Journal of Fluorine Chemistry, 183 (2016), 23
Ya. Dong, Q. Li, J. Wang, L. Lu, Yu. Wang, L. Bao, Zh. Wang, Yu. Zhang, “Chiral separation and quantitative analysis of citalopram by modified capillary electrophoresis”, Mendeleev Commun., 26:2 (2016), 166–168
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