Recent Progress on Transition Metal Catalyzed Macrocyclizations Based on C‐H Bond Activation at Heterocyclic Scaffolds

Abstract Macrocycles are essential in protein‐protein interactions and the preferential intake of bioactive scaffolds. Macrocycles are commonly synthesized by late‐stage macrolactonizations, macrolactamizations, transition metal‐catalyzed ring‐closing metathesis, S−S bond‐forming reactions, and copper‐catalyzed alkyne–azide cycloaddition. Recently, transition metal‐catalyzed C−H activation strategies have gained significant interest among chemists to synthesize macrocycles. This article provides a comprehensive overview of the transition metal‐catalyzed macrocyclization via C−H bond functionalization of heterocycle‐containing peptides, annulations, and heterocycle‐ring construction through direct C−H bond functionalization. In the first part, palladium salt catalyzed coupling with indolyl C(sp 3 )−H and C(sp 2 )−H bonds for macrocyclization is reported. The second part summarizes rhodium‐catalyzed macrocyclizations via site‐selective C−H bond functionalization. Earth‐abundant, less toxic 3d metal salt Mn‐catalyzed cyclizations are reported in the latter part. This summary is expected to spark interest in emerging methods of macrocycle production among organic synthesis and chemical biology practitioners, helping to develop the discipline. We hope that this mini‐review will also inspire synthetic chemists to explore new and broadly applicable C−C bond‐forming strategies for macrocyclization via intramolecular C−H activation.