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Light Promoted Vinylogous Arbuzov Reaction with Electron Deficient Alkyl Halides Научная публикация

Журнал Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052
Вых. Данные Год: 2025, Том: 27, Номер: 26, Страницы: 7106–7110 Страниц : DOI: 10.1021/acs.orglett.5c01993
Авторы Kostromitin Vladislav S. 1,2 , Supranovich Vyacheslav I. 2 , Dilman Alexander D. 2
Организации
1 Lomonosov Moscow State University, Department of Chemistry, Leninskie Gory 1-3, 119991 Moscow, Russian Federation
2 N. D. Zelinsky Institute of Organic Chemistry, Leninsky prosp. 47, 119991 Moscow, Russian Federation

Реферат: A vinylogous radical Arbuzov reaction involving the coupling of alkyl halides, terminal acetylenes, and triethyl phosphite furnishing vinyl phosphonates is described. Fluorinated iodides and α-bromoesters served as sources of radicals. The reaction is initiated by 400 nm light with or without photocatalyst, depending on the alkyl halide. The fluoroalkylation products could be further partially protodefluorinated using 1,3,5-trimethyltriazinane.
Библиографическая ссылка: Kostromitin V.S. , Supranovich V.I. , Dilman A.D.
Light Promoted Vinylogous Arbuzov Reaction with Electron Deficient Alkyl Halides
Organic Letters. 2025. V.27. N26. P.7106–7110. DOI: 10.1021/acs.orglett.5c01993 WOS OpenAlex
Идентификаторы БД:
Web of science: WOS:001518029500001
OpenAlex: W4411521770
Цитирование в БД: Пока нет цитирований
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