Cyclic Amine Synthesis via Catalytic Radical‐Polar Crossover Cycloadditions

The rapid assembly of valuable cyclic amine architectures in a single step from simple precursors has been recognized as an ideal platform in term of efficiency and sustainability. Although a vast number of studies regarding cyclic amine synthesis has been reported, new synthetic disconnection approaches are still high in demand. Herein, we report a catalytic radical‐polar crossover cycloaddition to cyclic amine synthesis triggered from primary sulfonamide under photoredox condition. This newly developed disconnection, comparable to established synthetic approaches, will allow to construct β, β‐disubstituted cyclic amine and β‐monosubstituted cyclic amine derivatives efficiently. This study highlights the unique utility of primary sulfonamide as a bifunctional reagent, which acts as a radical precursor and a nucleophile. The open‐shell methodology demonstrates broad tolerance to various functional groups, drug derivatives and natural products in an economically and sustainable fashion. Cyclic amine synthesis has been achieved by a catalytic radical‐polar crossover cycloaddition (RPCC) triggered from primary sulfonamide under photoredox condition. The newly developed disconnection allows to construct β, β‐disubstituted and β‐monosubstituted cyclic amines. This study highlights the unique utility of primary sulfonamides as bifunctional reagents, which act as radical precursors and nucleophiles.