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A new approach to polyfluoroaromatic amines with an unsubstituted position ortho to the amino group Научная публикация

Журнал Journal of Fluorine Chemistry
ISSN: 0022-1139
Вых. Данные Год: 2001, Том: 110, Номер: 1, Страницы: 43-46 Страниц : DOI: 10.1016/S0022-1139(01)00404-3
Ключевые слова reductive defluorination; hydrodefluorination; zinc; aqueous ammonia; polyfluoroaromatic amines; N-acetyl derivatives; acetamido group
Авторы Laev SS , Evtefeev VU , Shteingarts VD
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Div, NN Vorozhtsov Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

Реферат: N-acetyl derivatives of polyfluoroaromatic amines have been found to be highly selectively defluorinated by zinc in aqueous ammonia at the position ortho to the acetamido group thus affording a new approach to potential building blocks for the synthesis of polyfluorobenzheterocycles. (C) 2001 Elsevier Science B.V. All rights reserved.
Библиографическая ссылка: Laev S. , Evtefeev V. , Shteingarts V.
A new approach to polyfluoroaromatic amines with an unsubstituted position ortho to the amino group
Journal of Fluorine Chemistry. 2001. V.110. N1. P.43-46. DOI: 10.1016/S0022-1139(01)00404-3 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 июл. 2001 г.
Идентификаторы БД:
Web of science: WOS:000170257800008
Scopus: 2-s2.0-0034923836
РИНЦ: 13368461
OpenAlex: W2059633203
Цитирование в БД:
БД Цитирований
Web of science 27
Scopus 29
РИНЦ 29
OpenAlex 27
Альметрики: