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Mendeleev Communications, 2018, Volume 28, Issue 1, Pages 22–24
DOI: https://doi.org/10.1016/j.mencom.2018.01.005
(Mi mendc1649)
 

This article is cited in 3 scientific papers (total 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
Full-text PDF (220 kB) Citations (3)
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.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (489.4 Kb)


Citation: N. I. Guranova, A. V. Varlamov, R. A. Novikov, A. V. Aksenov, T. N. Borisova, E. A. Sorokina, L. G. Voskresenskii, “Reaction of benzyne with 1,2,3,4-tetrahydroisoquinolines as an access to 1H-3-benzazepines”, Mendeleev Commun., 28:1 (2018), 22–24
Linking options:
  • https://www.mathnet.ru/eng/mendc1649
  • https://www.mathnet.ru/eng/mendc/v28/i1/p22
  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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