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Skraup-like cyclization of polyfluoro-2-naphthylamines: Vicarious electrophilic substitution of fluorine Full article

Journal Journal of Fluorine Chemistry
ISSN: 0022-1139
Output data Year: 2012, Volume: 137, Pages: 113-116 Pages count : DOI: 10.1016/j.jfluchem.2012.03.001
Tags Bolyfluoro-2-naphthylamines; Skraup-like cyclization; Glycerol; Polyfluorobenzo[f]quinolines; Vicarious electrophilic substitution of fluorine
Authors Selivanova Galina A. 1 , Reshetov Alexey V. 1 , Bagryanskaya Irina Yu 1 , Shteingarts Vitalij D. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Div, NN Vorozhtsov Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: Treatment of polyfluoro-2-naphthylamines with glycerol in H2SO4 or CF3SO3H at 150-160 degrees C gives respective polyfluorobenzo[f]quinolines. The reaction is suggested to proceed via intramolecular vicarious electrophilic substitution of fluorine at the alpha-position of polyfluorinated naphthalene core. (c) 2012 Elsevier B.V. All rights reserved.
Cite: Selivanova G.A. , Reshetov A.V. , Bagryanskaya I.Y. , Shteingarts V.D.
Skraup-like cyclization of polyfluoro-2-naphthylamines: Vicarious electrophilic substitution of fluorine
Journal of Fluorine Chemistry. 2012. V.137. P.113-116. DOI: 10.1016/j.jfluchem.2012.03.001 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: May 1, 2012
Identifiers:
Web of science: WOS:000304179700016
Scopus: 2-s2.0-84859575470
Elibrary: 17982304
OpenAlex: W2000756537
Citing:
DB Citing
Web of science 3
Scopus 3
Elibrary 3
OpenAlex 4
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