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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2018 Volume 28, Issue 1, Pages 22–24 (Mi mendc1649)

This article is cited in 3 papers

Communications

Reaction of benzyne with 1,2,3,4-tetrahydroisoquinolines as an access to 1H-3-benzazepines

N. I. Guranovaa, A. V. Varlamova, R. A. Novikovb, A. V. Aksenovc, T. N. Borisovaa, E. A. Sorokinaa, L. G. Voskresenskiia

a Peoples Friendship University of Russia (RUDN University), Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c Department of Biology and Chemistry, Stavropol State University, Stavropol, Russian Federation

Abstract: 1,2,3,4-Tetrahydroisoquinolines bearing phenacyl group at the nitrogen atom in their reaction with benzyne in acetonitrile undergo ring expansion to give 1H-3-benzazepines.

Language: English

DOI: 10.1016/j.mencom.2018.01.005



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