Photoinduced Assembly of Diverse Homoallylic Boronates from -Diborons.

In comparison to alkyl monoboron or 1,2-diboron, which can generate alkyl radicals via tetracoordinate boron species under photocatalytic conditions, the participation of -diborons as substrates in such reactions remains to be developed. Herein, we report a method utilizing -diborons as starting materials to generate α-boryl radicals, which then react with various olefins, successfully and efficiently constructing a diverse range of high-value homoallylic boronates; meanwhile, the -difluorohomoallylic skeletons could also be smoothly obtained. This transformation demonstrates broad substrate scope and excellent tolerance toward functional groups, enhancing the utility of -diboron as precursors for C-C bond construction and the production of valuable products.