摘要 : Abstract Selective C(sp2)?H bond alkylation of indoline, carbazole and (2‐pyridinyl)arenes with unactivated alkyl bromides is achieved using MnBr2 catalyst in the absence of an external ligand. The alkylation uses a simple LiHMDS... 展开 Abstract Selective C(sp2)?H bond alkylation of indoline, carbazole and (2‐pyridinyl)arenes with unactivated alkyl bromides is achieved using MnBr2 catalyst in the absence of an external ligand. The alkylation uses a simple LiHMDS base and avoids the necessity of Grignard reagent, unlike other Mn‐catalyzed C?H functionalization. This reaction proceeded either through a five‐ or a less‐favored six‐membered metallacycle, and tolerated diverse functionalities, including alkenyl, alkynyl, silyl, aryl ether, pyrrolyl, indolyl, carbazolyl and alkyl bearing fatty alcohol and polycyclic‐steroid moieties. Alkylation follows a single electron transfer (SET) pathway involving 1e oxidative addition of alkyl bromide and a rate‐limiting C?H metalation. 收起