Abstract
A new and powerful visible-light-induced difunctionalization of the C-C σ-bond of alkylidenecyclopropanes via a ring-opening process was developed. Importantly, acyl chlorides are used as both acyl and Cl sources. This strategy provides an effective route for the difunctionalization of the C-C bond with an acyl radical and Cl− to construct a new C-C bond and a C-Cl bond in one pot. In addition, it has a wide range of substrates and can tolerate various functional groups.
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