Activation of perfluoroalkyl iodides by anions: extending the scope of halogen bond activation to C(sp 3 )-H amidation, C(sp 2 )-H iodination, and perfluoroalkylation reactions.

A simple, efficient, and convenient activation of perfluoroalkyl iodides by t BuONa or KOH, without expensive photo- or transition metal catalysts, allows the promotion of versatile α-sp 3 C-H amidation reactions of alkyl ethers and benzylic hydrocarbons, C-H iodination of heteroaryl compounds, and perfluoroalkylations of electron-rich π bonds. Mechanistic studies show that these novel protocols are based on the halogen bond interaction between perfluoroalkyl iodides and t BuONa or KOH, which promote homolysis of perfluoroalkyl iodides under mild conditions.