Catalytic enantioselective synthesis of α-C chiral sulfones enabled by merging photoactive electron donor-acceptor complexes with nickel catalysis.
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ABSTRACT: α-C chiral sulfones are privileged building blocks widely found in pharmaceuticals, agrochemicals, natural products, and ligands. Although many nucleophilic or electrophilic protocols have been developed for their construction, radical-based asymmetric catalysis, especially that involving photoactive electron donor-acceptor (EDA) complexes, remains a significant unmet challenge. Herein, we present the first catalytic asymmetric production of α-C chiral sulfones enabled by merging a photoactive EDA complex with a chiral Ni catalyst. With this cooperative asymmetric catalysis system, a wide range of α-C chiral sulfones are achieved in good yields with excellent enantioselectivities (53 examples, up to 99% yield, 99 : 1 er). The synthetic utility of this protocol is further demonstrated by th
SUBMITTER: Lai ZM
PROVIDER: S-EPMC11793018 | biostudies-literature | 2025 Mar
REPOSITORIES: biostudies-literature
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