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

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

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.

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

Published print:

Jul 1, 2001

Web of science	WOS:000170257800008
Scopus	2-s2.0-0034923836
Elibrary	13368461
OpenAlex	W2059633203