Visible-Light-Promoted Regioselective 1,3-Fluoroallylation of gem-Difluorocyclopropanes

A strategically novel protocol for ring-opening functionalization of aryl gem-difluorocyclopropanes (F₂CPs), which allows an expedient construction of CF₃-containing architectures via visible-light-promoted F-nucleophilic attack manifold, was disclosed. Single electron oxidation of F₂CPs was ascribed as the critical step for the success of this transformation by prompting F-nucleophilic attack, as well as the ensuing C−C bond scission. The observed intriguing regioselectivity for fluoroincorporation in this reaction was rationalized by invoking the cation-stabilization property of gem-difluorine substituents and also the thermodynamic gains acquired from forming CF₃ functionality. By using cost-effective fluorination reagent and readily available substrates, a broad collection of structurally diversified α-allyl-β-trifluoromethyl ethylbenzene derivatives could be obtained in generally good yields. Further mechanistic investigations proved the engagement of a benzylic radical intermediate in this transformation.