Add time:08/06/2019 Source:sciencedirect.com
Treatment of nitroarenes with 1-(phenylsulphonylmethyl)azoles in the KOH/DMSO system at room temperature resulted usually in the cleavage of the phenylsulphonyl group, whereas the t-BuOK/DMF system at low temperature promotes to a greater extent oxidation of the σ-adducts. When 1-(phenylsulphinylmethyl)azoles were used for the reaction only elimination of the phenylsulphinyl group was observed.
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