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

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. © 2018

Авторы
Guranova N.I. 1 , Varlamov A.V. 1 , Novikov R.A. 2 , Aksenov A.V. 3 , Borisova T.N. 1 , Sorokina E.A. 1 , Voskressensky L.G. 1
Журнал
Mendeleev Communications
Издательство
Royal Society of Chemistry
Номер выпуска
1
Язык
Английский
Страницы
22-24
Статус
Опубликовано
Ссылка
Внешняя ссылка
DOI
10.1016/J.MENCOM.2018.01.005
Том
28
Год
2018
Организации
  • 1 Organic Chemistry Department, Peoples Friendship University of Russia (RUDN University), Moscow, 117198, Russian Federation
  • 2 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, 119991, Russian Federation
  • 3 North-Caucasus Federal University, Stavropol, 355009, Russian Federation
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