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 |
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| 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 |
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| Организации |
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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
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
Даты:
| Опубликована в печати: | 1 июл. 2001 г. |
Идентификаторы:
| Web of science | WOS:000170257800008 |
| Scopus | 2-s2.0-0034923836 |
| РИНЦ | 13368461 |
| OpenAlex | W2059633203 |