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SELECTIVE ORTHO-ARYLATION OF POLYFLUORINATED HYDROXYAROMATIC COMPOUNDS WITH LEAD ARYL ACETATES Научная публикация

Журнал Journal of Fluorine Chemistry
ISSN: 0022-1139
Вых. Данные Год: 1993, Том: 63, Номер: 3, Страницы: 243-251 Страниц : 9 DOI: 10.1016/S0022-1139(00)80568-0
Авторы Kovtonyuk V.N. 1 , Kobrina L.S. 1
Организации
1 Institute of Organic Chemistry, Novosibirsk 630090 Russian Federation

Реферат: Reactions of salts of pentafluorophenol and heptafluoronaphthols with lead aryl acetates have led to the formation of arylcyclohexadienones with an ortho-quinoid structure. The arylation of sodium pentafluorophenoxide and heptafluoro-2-naphthoxide is accompanied by nucleophilic substitution of fluorine at a double bond by pentafluorophenoxy and heptafluoro-2-naphthoxy groups, respectively. Reduction of the resulting arylcyclohexadienones gave polyfluorinated phenols and naphthols with aryl and hydroxy groups in the 1,2-position.
Библиографическая ссылка: Kovtonyuk V.N. , Kobrina L.S.
SELECTIVE ORTHO-ARYLATION OF POLYFLUORINATED HYDROXYAROMATIC COMPOUNDS WITH LEAD ARYL ACETATES
Journal of Fluorine Chemistry. 1993. V.63. N3. P.243-251. DOI: 10.1016/S0022-1139(00)80568-0 WOS Scopus OpenAlex
Даты:
Опубликована в печати: 1 авг. 1993 г.
Идентификаторы БД:
Web of science: WOS:A1993LP18800007
Scopus: 2-s2.0-0010775564
OpenAlex: W2005980715
Цитирование в БД:
БД Цитирований
Web of science 9
Scopus 10
OpenAlex 11
Альметрики: