Ruthenium(II)-Catalyzed Oxidative CH Alkenylations of Sulfonic Acids, Sulfonyl Chlorides and Sulfonamides

Twofold CH functionalization of aromatic sulfonic acids was achieved with an in situ generated ruthenium(II) catalyst. The optimized cross‐dehydrogenative alkenylation protocol proved applicable to differently substituted arenes and a variety of alkenes, including vinyl arenes, sulfones, nitriles and ketones. The robustness of the ruthenium(II) catalyst was demonstrated by the chemoselective oxidative olefination of sulfonamides as well as sulfonyl chlorides. Mechanistic studies provided support for a reversible, acetate‐assisted CH ruthenation, along with a subsequent olefin insertion. Versatile oxidative alkenylations of sulfonic acids, sulfonyl chlorides or sulfonamides were achieved by a robust ruthenium(II) catalyst with excellent substrate scope. Mechanistic studies suggested a reversible, acetate‐assisted CH ruthenation, along with a subsequent olefin insertion.