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Transformations of perfluoroxylenes and perfluoro-p-cymene under the action of Zn(Cu)-DMF-H2O. Full article

Journal Tetrahedron
ISSN: 0040-4020
Output data Year: 1997, Volume: 53, Number: 5, Pages: 1797-1812 Pages count : 16 DOI: 10.1016/S0040-4020(96)01090-3
Authors Krasnov V.I. 1 , Platonov V.E. 1 , Beregovaya I.V. 1 , Shchegoleva L.N. 1
Affiliations
1 Institute of Organic Chemistry, Novosibirsk, 630090, Russia

Abstract: Perfluorinated xylenes and perfluoro-para-cymene undergo hydrodefluorination under the action of Zn(Cu)-DMF-H2O. Hydrogen enters mainly at the benzyl position of para-dialkylbenzenes and at the para position to perfluoroalkyl groups of perfluorinated ortho- and meta-xylenes. The process presumably involves radical anions as intermediates. A product of perfluoro-4-methylbenzyl radical trapping by hexene-1 was obtained Quantum-chemical calculations of radical anions of the compounds under investigation have been carried out. (C) 1997, Elsevier Science Ltd.
Cite: Krasnov V.I. , Platonov V.E. , Beregovaya I.V. , Shchegoleva L.N.
Transformations of perfluoroxylenes and perfluoro-p-cymene under the action of Zn(Cu)-DMF-H2O.
Tetrahedron. 1997. V.53. N5. P.1797-1812. DOI: 10.1016/S0040-4020(96)01090-3 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Feb 1, 1997
Identifiers:
Web of science: WOS:A1997WF28300027
Scopus: 2-s2.0-0031550585
Elibrary: 13259657
OpenAlex: W1967221220
Citing:
DB Citing
Web of science 21
Scopus 21
Elibrary 25
OpenAlex 27
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