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Asymmetric synthesis of warfarin and its analogs catalyzed by C2-symmetric squaramide-based primary diamines Научная публикация

Журнал Organic & Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539
Вых. Данные Год: 2018, Том: 16, Номер: 35, Страницы: 6423-6429 Страниц : 7 DOI: 10.1039/c8ob01576g
Авторы Kochetkov Sergei Viktorovich 1 , Kucherenko Alexander 1 , Zlotin Sergei Grigorievich 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russia

Реферат: Novel C2-symmetric N,N′-bis(2-amino-1,2-diphenylethyl)squaramides with 1,2-di(pyridin-2-yl)ethane and 1,2-diphenylethane spacer groups were designed and applied as organocatalysts in asymmetric additions of 4-hydroxycoumarin and 4-hydroxy-6-methyl-2H-pyran-2-one to α,β-unsaturated ketones. Both enantiomers of the anticoagulant warfarin and its analogs were prepared in up to 96% yield and with 96% ee. Recyclability of the developed catalysts and synthetic utility of the prepared Michael adducts for asymmetric synthesis of potential chiral medications via acylation reactions were demonstrated.
Библиографическая ссылка: Kochetkov S.V. , Kucherenko A. , Zlotin S.G.
Asymmetric synthesis of warfarin and its analogs catalyzed by C2-symmetric squaramide-based primary diamines
Organic & Biomolecular Chemistry. 2018. V.16. N35. P.6423-6429. DOI: 10.1039/c8ob01576g WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000444484800007
Scopus: 2-s2.0-85053526611
OpenAlex: W2883059706
Цитирование в БД:
БД Цитирований
OpenAlex 16
Scopus 16
Web of science 17
Альметрики: