Chemical diversity of pyrrolobenzazepine derivatives with a nodal nitrogen atom

Five-, six- and seven-membered carbo- and heterocycles are widespread in nature, and their tricyclic combinations can form a broad spectrum of complex molecules exhibiting unique properties. In the present review we have covered the known synthetic approaches towards tricyclic pyrrolobenzazepine derivatives with a nodal nitrogen atom and described some of their biological activities. Herein, we present systematized information on four skeletally isomeric scaffolds: pyrrolo[2,1-b][3]benzazepines, pyrrolo[1,2-b][2]benzazepines, pyrrolo[2,1-a][2]benzazepines, and pyrrolo[1,2-a][1]benzazepines. © 2025 Elsevier B.V., All rights reserved.

Издательство
Elsevier Science Publishing Company, Inc.
Язык
English
Статус
Published
Номер
134524
Том
176
Год
2025
Организации
  • 1 Department of Organic Chemistry, RUDN University, Moscow, Russian Federation
Ключевые слова
Heck reaction; Photochemical transformations; Pyrrolo[1,2-a][1]benzazepines; Pyrrolo[1,2-b][2]benzazepines; Pyrrolo[2,1-a][2]benzazepines; Pyrrolo[2,1-b][3]benzazepines; Sigmatropic rearrangements
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