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Revision of the scheme for the formation of heterocyclic quinones upon the photolysis of 3-amino-2-cycloalkylamino-1,4-naphthoquinones
Authors:V N Berezhnaya  R P Shishkina  E P Fokin
Institution:(1) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, USSR
Abstract:Conclusions The formation of naphthimidazole derivatives in the photolysis of 3-amino- and 3-acetyl-amino-2-cycloalkylamino-1,4-naphthoquinones is the result of the dark intramolecular cyclization of the corresponding 3-aminoenaminoquinones.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 694–699, March, 1989.
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