Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer.

Chem Sci

Max-Planck-Institut für Kohlenforschung Kaiser-Wilhelm Platz 1 D-45470 Mülheim an der Ruhr Germany

Published: November 2022

Sulfoximines are synthetically important scaffolds and serve important roles in drug discovery. Currently, there is no solution to decarboxylative sulfoximination of benzoic acids; although thoroughly investigated, limited substrate scope and harsh reaction conditions still hold back traditional thermal aromatic decarboxylative functionalization. Herein, we realize the first decarboxylative sulfoximination of benzoic acids photo-induced ligand to copper charge transfer (copper-LMCT)-enabled decarboxylative carbometalation. The transformation proceeds under mild reaction conditions, has a broad substrate scope, and can be applied to late-stage functionalization of complex small molecules.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682917PMC
http://dx.doi.org/10.1039/d2sc05442fDOI Listing

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Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer.

Chem Sci

November 2022

Max-Planck-Institut für Kohlenforschung Kaiser-Wilhelm Platz 1 D-45470 Mülheim an der Ruhr Germany

Sulfoximines are synthetically important scaffolds and serve important roles in drug discovery. Currently, there is no solution to decarboxylative sulfoximination of benzoic acids; although thoroughly investigated, limited substrate scope and harsh reaction conditions still hold back traditional thermal aromatic decarboxylative functionalization. Herein, we realize the first decarboxylative sulfoximination of benzoic acids photo-induced ligand to copper charge transfer (copper-LMCT)-enabled decarboxylative carbometalation.

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