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Synthesis of perfluorinated biaryls by reaction of perfluoroarylzinc compounds with perfluoroarenes Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2015, Volume: 51, Number: 10, Pages: 1388-1394 Pages count : 7 DOI: 10.1134/S107042801510005X
Authors Vinogradov A.S. 1 , Platonov V.E. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

Abstract: Symmetrical and unsymmetrical perfluorinated biaryls have been synthesized by reactions of perfluorinated benzonitrile, nitrobenzene, toluene, m-xylene, and pyridine with perfluoroarylzinc compounds derived from chloropentafluorobenzene, octafluorotoluene, and pentafluoropyridine. The described transformations may be regarded as nucleophilic aromatic substitution.
Cite: Vinogradov A.S. , Platonov V.E.
Synthesis of perfluorinated biaryls by reaction of perfluoroarylzinc compounds with perfluoroarenes
Russian Journal of Organic Chemistry. 2015. V.51. N10. P.1388-1394. DOI: 10.1134/S107042801510005X WOS Scopus РИНЦ OpenAlex
Original: Виноградов А.С. , Платонов В.Е.
Синтез перфтордиарилов действием перфторарилцинкорганических соединений на перфторарены
Журнал органической химии (RUSS J ORG CHEM+). 2015. Т.51. №10. С.1419-1425. РИНЦ
Dates:
Published print: Oct 1, 2015
Published online: Nov 15, 2015
Identifiers:
Web of science: WOS:000365218700005
Scopus: 2-s2.0-84947444986
Elibrary: 24971830
OpenAlex: W2307167001
Citing:
DB Citing
Web of science 9
Scopus 7
Elibrary 9
OpenAlex 8
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