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Synthesis of Polyfluorinated 4-Phenyl-3,4-Dihydroquinolin-2-ones and Quinolin-2-ones via Superacidic Activation of N-(polyfluorophenyl)cinnamamides Научная публикация

Журнал Tetrahedron Letters
ISSN: 0040-4039
Вых. Данные Год: 2009, Том: 50, Номер: 37, Страницы: 5245-5247 Страниц : 3 DOI: 10.1016/j.tetlet.2009.07.013
Ключевые слова Fluoroquinolines, Fluoroquinolinones, Lewis acid, Polyfluoroanilides, Superacids, Superelectrophiles
Авторы Safina Larisa Yu. 1 , Selivanova Galina A. 1 , Koltunov Konstantin Yu. 2,3 , Shteingarts Vitalij D. 1,3
Организации
1 N.N. Vorozhtsov Institute of Organic Chemistry, Siberian Division of the Russian Academy of Sciences, 9 Ac. Lavrentjev Avenue, Novosibirsk 630090, Russia
2 G.K. Boreskov Institute of Catalysis, Siberian Division of the Russian Academy of Sciences, 5 Ac. Lavrentjev Avenue, Novosibirsk 630090, Russia
3 Novosibirsk State University, Pirogova Str., 2, Novosibirsk 630090, Russia

Информация о финансировании (2)

1 Российский фонд фундаментальных исследований 00-03-40142
2 Российский фонд фундаментальных исследований 09-03-00248

Реферат: The cyclization reactions of a series of polyfluorocinnamanilides in triflic acid (CF3SO3H) yield 4-phenyl-3,4-dihydroquinolin-2-ones, which include a polyfluorinated benzene moiety as a part of the quinoline scaffold. These compounds undergo dehydrophenylation in the presence of AlCl3 to give the corresponding polyfluoroquinolin-2-ones which are converted into polyfluorinated 2-chloroquinolines on treatment with POCl3. A mechanism for the cyclization reaction presuming the intermediacy of a superelectrophilic O,C-diprotonated form of the starting material is suggested.
Библиографическая ссылка: Safina L.Y. , Selivanova G.A. , Koltunov K.Y. , Shteingarts V.D.
Synthesis of Polyfluorinated 4-Phenyl-3,4-Dihydroquinolin-2-ones and Quinolin-2-ones via Superacidic Activation of N-(polyfluorophenyl)cinnamamides
Tetrahedron Letters. 2009. V.50. N37. P.5245-5247. DOI: 10.1016/j.tetlet.2009.07.013 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 22 апр. 2009 г.
Принята к публикации: 3 июл. 2009 г.
Опубликована online: 9 июл. 2009 г.
Опубликована в печати: 16 сент. 2009 г.
Идентификаторы БД:
Web of science: WOS:000269051700021
Scopus: 2-s2.0-67650918373
РИНЦ: 13614228
Chemical Abstracts: 2009:905536
Chemical Abstracts (print): 151:403087
OpenAlex: W1988112731
Цитирование в БД:
БД Цитирований
Web of science 25
Scopus 25
РИНЦ 25
OpenAlex 22
Альметрики: