
Synlett, Journal Year: 2025, Volume and Issue: unknown
Published: March 20, 2025
Abstract A new synthetic method has been established to synthesize α-carbolines through the reaction of electrophilic azaindoles with ambiphilic alkylidene malononitriles. The versatility this approach was explored by using various malononitriles, and also conducting nitrogen migration on azaindole. This enables simultaneous introduction diverse functional groups, such as amine, nitrile, aryl, onto benzene ring a carboline scaffold. As scaffold putatively shows antiproliferative other biological activities, is valuable in development chemical entities for drug discovery.
Language: Английский