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Ortho-hydrodefluorination of polyfluorinated 4-acetamidobiphenyls and synthesis of polyfluorinated 6-phenylquinolines Full article

Journal Journal of Fluorine Chemistry
ISSN: 0022-1139
Output data Year: 2013, Volume: 156, Pages: 214-219 Pages count : DOI: 10.1016/j.jfluchem.2013.09.015
Tags Zinc; Nickel complexes; Catalytic hydrodefluorination; 4-Acetamidononafluorobiphenyl; 4,4 '-Bis(acetamido)octafluorobiphenyl; Polyfluorinated 6-arylquinolines
Authors Gurskaya L. Yu 1 , Shteingarts V. D. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

Abstract: Polyfluorinated 4-acetamido- and 4,4'-bis(acetamido)biphenyl were reduced in the Zn-NiCl2-2,2'-bipyridine-aq. DMF system to give their for the first time synthesized less fluorinated analogs containing one or two unsubstituted position ortho to the acetamido group. By involving ortho-unsubstituted 4-acetamido- or 4-aminopolyfluorobiphenyis in the Skraup synthesis, new polyfluorinated 6-phenylquinolines and 6,6'-biquinoline were obtained. (C) 2013 Elsevier B.V. All rights reserved.
Cite: Gurskaya L.Y. , Shteingarts V.D.
Ortho-hydrodefluorination of polyfluorinated 4-acetamidobiphenyls and synthesis of polyfluorinated 6-phenylquinolines
Journal of Fluorine Chemistry. 2013. V.156. P.214-219. DOI: 10.1016/j.jfluchem.2013.09.015 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Dec 1, 2013
Identifiers:
Web of science: WOS:000329257000034
Scopus: 2-s2.0-84887074473
Elibrary: 21887220
OpenAlex: W2079587948
Citing:
DB Citing
Web of science 1
Scopus 1
Elibrary 1
OpenAlex 1
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