Chemistry Letters p. 1499 - 1502 (1987)
Update date:2022-08-16
Topics:
KIM, Yong Hae
LEE, Hyeon Kyu
Various sulfoxides, such as dialkyl, alkyl-aryl, and diaryl sulfoxides, were readily oxidized into the corresponding sulfones, in excellent yields under mild conditions, by 2-nitrobenzene peroxysulfur intermediate generated in situ from 2-nitrobenzene-sulfonyl chloride and potassium superoxide at -30 deg C, in dry acetonitrile.Chemoselective oxidation of sulfoxides which contain both double bond and sulfinyl moiety to the sulfones, was observed under the same conditions.
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