A titanium(III)-catalyzed desulfonylation gives access to functionalized alkyl nitrile building blocks from α-sulfonyl nitriles, circumventing traditional base-mediated α-alkylation conditions and strong single electron donors. The reaction tolerates numerous functional groups including free alcohols, esters, amides, and it can be applied also to the α-desulfonylation of ketones. In addition, a one-pot desulfonylative alkylation is demonstrated. Preliminary mechanistic studies indicate a catalyst-dependent mechanism involving a homolytic C−S cleavage.
CITATION STYLE
Kern, C., Selau, J., & Streuff, J. (2021). A Titanium-Catalyzed Reductive α-Desulfonylation. Chemistry - A European Journal, 27(20), 6178–6182. https://doi.org/10.1002/chem.202005400
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