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Reactions of polyfluorinated 2,5-cyclohexadienones at the carbonyl group Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Вых. Данные Год: 1996, Том: 45, Номер: 7, Страницы: 1688-1691 Страниц : 4 DOI: 10.1007/BF01431808
Ключевые слова polyfluorinated cyclohexadienones; arylhydrazines; azobenzenes; organometallic compounds
Авторы Kovtonyuk V.N. 1 , Kobrina L.S. 1
Организации
1 Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 prosp, Akad. Lavrent eva, 630090, Novosibirsk, Russian Federation

Реферат: Perfluoro-4-phenoxy-2,5-cyclohexadienone reacts with phenyl- and pentafluorophenylhydrazines to give products of nucleophilic substitution of the fluorine atom at the double bond, 3-arylazotetrafluorophenols. In the presence of aluminum chloride, the reactions proceed at the carbonyl groups of polyfluorinated cyclohexadienones to form the corresponding polyfluorinated azobenzenes. Perfluoro-4-phenoxy-2,5-cyclohexadienone reacts with butyllithium and butylmagnesium bromides to give the product of addition at the carbonyl group.
Библиографическая ссылка: Kovtonyuk V.N. , Kobrina L.S.
Reactions of polyfluorinated 2,5-cyclohexadienones at the carbonyl group
Russian Chemical Bulletin. 1996. V.45. N7. P.1688-1691. DOI: 10.1007/BF01431808 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 июл. 1996 г.
Идентификаторы БД:
Web of science: WOS:A1996WF53700028
Scopus: 2-s2.0-0042283267
РИНЦ: 13230999
OpenAlex: W1970293788
Цитирование в БД:
БД Цитирований
Web of science 1
Scopus 1
РИНЦ 1
Альметрики: