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Nucleophilic substitutions in 6,7-difluoroquinoxalines Full article

Journal Journal of Fluorine Chemistry
ISSN: 0022-1139
Output data Year: 2001, Volume: 107, Number: 1, Pages: 71-80 Pages count : 10 DOI: 10.1016/S0022-1139(00)00345-6
Tags fluoroquinoxalines; synthesis; H-1, C-13 and F-19 NMR
Authors Charushin VN 1 , Mokrushina GA 1 , Tkachev AV 2
Affiliations
1 (Данные Web of science) Urals State Tech Univ, Dept Organ Chem, Sverdlovsk 620002, Russia
2 (Данные Web of science) Novosibirsk Organ Chem Inst, Novosibirsk 630090, Russia

Abstract: The reactions of 6.7-difluoroquinoxalines with a number of nucleophiles, such as cycloalkylimines. hydrazine, sodium hydroxide and alkoxides have been shown to result in substitution of either one or two fluoro atoms depending on the nature of nucleophiles. (C) 2001 Elsevier Science B.V. All rights reserved.
Cite: Charushin V. , Mokrushina G. , Tkachev A.
Nucleophilic substitutions in 6,7-difluoroquinoxalines
Journal of Fluorine Chemistry. 2001. V.107. N1. P.71-80. DOI: 10.1016/S0022-1139(00)00345-6 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Jan 1, 2001
Identifiers:
Web of science: WOS:000166676200012
Scopus: 2-s2.0-0035182003
Elibrary: 13378981
OpenAlex: W2028561972
Citing:
DB Citing
Web of science 13
Scopus 15
Elibrary 16
OpenAlex 16
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