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
Сохранить в:
相似书籍
-
Reactions of 3,4-dihydroisoquinolines and dihydrothieno[3,2-c]pyridines with benzyne
由: Aksenov, A. V., и др.
出版: (2018) -
Direct C-H functionalization of arenes in reactions with nitroalkanes and nitroalkenes in polyphosphoric acids
由: Aksenov, A. V., и др.
出版: (2019) -
Domino reactions of 1-substituted N-(cyanomethyl)isoquinolinium salts with salicylic aldehydes
由: Aksenov, A. V., и др.
出版: (2018) -
Modeling stages of domino reaction of thiopyrano[4,3-b]indole-3(5H)-thiones and dimethyl acetylenedicarboxylate: a new synthetic route to γ-carbolines with thione group
由: Demidov, O. P., и др.
出版: (2024) -
Substrate-dependent regiodivergent three-component condensation of 1H-pyrrole-2,3-diones, malononitrile and 4-hydroxyquinolin-2(1H)-ones
由: Rubin, M. A., и др.
出版: (2021)