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Эта публикация цитируется в 6 научных статьях (всего в 6 статьях)
Solid-state properties of 1,2-epoxy-3-(2-cyanophenoxy)propane, a conglomerate-forming chiral drug precursor
A. A. Bredikhin, Z. A. Bredikhina, D. V. Zakharychev, F. S. Akhatova, D. B. Krivolapov, I. A. Litvinov
A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
Аннотация:
Both enantiomers of 1,2-epoxy-3-(2-cyanophenoxy)propane 1a were obtained and converted into enantiomeric bunitrolol hydrochlorides 3 to confirm the configuration of the formers; racemic 1a undergoes spontaneous resolution upon crystallization and could be resolved into individual enantiomers by a preferential crystallization with low efficiency.
Образец цитирования:
A. A. Bredikhin, Z. A. Bredikhina, D. V. Zakharychev, F. S. Akhatova, D. B. Krivolapov, I. A. Litvinov, “Solid-state properties of 1,2-epoxy-3-(2-cyanophenoxy)propane, a conglomerate-forming chiral drug precursor”, Mendeleev Commun., 16:5 (2006), 245–247
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3607 https://www.mathnet.ru/rus/mendc/v16/i5/p245
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