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A new approach to polyfluoroaromatic amines with an unsubstituted position ortho to the amino group Full article

Journal Journal of Fluorine Chemistry
ISSN: 0022-1139
Output data Year: 2001, Volume: 110, Number: 1, Pages: 43-46 Pages count : DOI: 10.1016/S0022-1139(01)00404-3
Tags reductive defluorination; hydrodefluorination; zinc; aqueous ammonia; polyfluoroaromatic amines; N-acetyl derivatives; acetamido group
Authors Laev SS , Evtefeev VU , Shteingarts VD
Affiliations
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

Abstract: 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.
Cite: 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
Dates:
Published print: Jul 1, 2001
Identifiers:
Web of science: WOS:000170257800008
Scopus: 2-s2.0-0034923836
Elibrary: 13368461
OpenAlex: W2059633203
Citing:
DB Citing
Web of science 27
Scopus 29
Elibrary 29
OpenAlex 27
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