Mendeleev Commun., 2018, том 28, выпуск 1, страницы 22–24
(Mi mendc1649)
Эта публикация цитируется в
3 статьях
Reaction of benzyne with 1,2,3,4-tetrahydroisoquinolines as an access to 1H-3-benzazepines
N. I. Guranova a ,
A. V. Varlamov a ,
R. A. Novikov b ,
A. V. Aksenov c ,
T. N. Borisova a ,
E. A. Sorokina a ,
L. G. Voskresenskii a 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
Аннотация:
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.
Ключевые слова:
tetrahydroisoquinolines, benzyne, benzoazepines, Stevens rearrangement, aryne.
Язык публикации: английский
DOI:
10.1016/j.mencom.2018.01.005
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