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Highly Regioselective Nickel-Catalyzed Hydrodefluorination of Pentafluoroacetanilide Full article

Journal Mendeleev Communications
ISSN: 0959-9436 , E-ISSN: 1364-551X
Output data Year: 2008, Volume: 18, Number: 4, Pages: 211-212 Pages count : 2 DOI: 10.1016/j.mencom.2008.07.015
Tags CARBON-FLUORINE BOND; SC-F BONDS; AQUEOUS AMMONIA; HYDROGENOLYSIS; ACTIVATION; COMPLEXES; DEFLUORINATION; ZINC
Authors Prikhodʹko Sergey A. 1 , Adonin Nicolay Yu. 1 , Babushkin Dmitrii E. 1 , Parmon Valentin N. 1
Affiliations
1 G. K. Boreskov Institute of Catalysis, Siberian Branch, the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

Funding (1)

1 Президиум РАН 5.8.5

Abstract: A highly regioselective reaction of pentafluoroacetanilide hydrodefluorination, which proceeds under the action of zinc in the presence of nickel complexes, leading to the formation of 2,3,4,5-tetra- and 3,4,5-trifluoroacetanilide was observed.
Cite: Prikhodʹko S.A. , Adonin N.Y. , Babushkin D.E. , Parmon V.N.
Highly Regioselective Nickel-Catalyzed Hydrodefluorination of Pentafluoroacetanilide
Mendeleev Communications. 2008. V.18. N4. P.211-212. DOI: 10.1016/j.mencom.2008.07.015 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Jan 23, 2008
Published print: Jul 1, 2008
Published online: Aug 9, 2008
Identifiers:
Web of science: WOS:000259340300015
Scopus: 2-s2.0-48749086845
Elibrary: 13575678
Chemical Abstracts: 2008:1142918
Chemical Abstracts (print): 150:398095
OpenAlex: W2124968436
Citing:
DB Citing
Web of science 21
Scopus 22
Elibrary 21
OpenAlex 25
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