Ortho-hydrodefluorination of polyfluorinated 4-acetamidobiphenyls and synthesis of polyfluorinated 6-phenylquinolines Full article
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Journal of Fluorine Chemistry
ISSN: 0022-1139 |
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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 | ||
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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
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
Dates:
Published print: | Dec 1, 2013 |
Identifiers:
Web of science | WOS:000329257000034 |
Scopus | 2-s2.0-84887074473 |
Elibrary | 21887220 |
OpenAlex | W2079587948 |