Direct C-H Methylsulfonylation of Alkenes with the Insertion of Sulfur Dioxide
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Updated: Jan 19, 2026
Biogeochemical Cycles: the Sulfur Cycle
Fu-Sheng He1, Xinxing Gong2, Pornchai Rojsitthisak3
1School of Pharmaceutical and Materials Engineering and Institute for Advanced Studies , Taizhou University , 1139 Shifu Avenue , Taizhou 318000 , China.
Abstract:
The direct C-H methylsulfonylation of alkenes using inorganic sodium metabisulfite as the sulfur dioxide surrogate is described. This method provides convenient access to (E)-2-methyl styrenyl sulfones in good yields. In general, the in situ generated methyl radical from di-tert-butyl peroxide undergoes a methylsulfonylation process with the combination of sulfur dioxide.
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