Intramolecular cascade annulation triggered by rhodium(III)catalyzed sequential C(sp2)–H activation and C(sp3)–H amination

Abstract

A rhodium(III)-catalyzed intramolecular oxidative annulation of O-substituted N-hydroxyacrylamides for the construction of indolizinones via sequential C(sp2)–H activation and C(sp3)–H amination has been developed. This approach shows excellent functional-group tolerance. The synthesized scaffold forms the core of many natural products with pharmacological relevance.