Journal
ORGANIC LETTERS
Volume 21, Issue 13, Pages 4950-4954Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b01323
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Funding
- National Natural Science Foundation of China [21672037, 21532001]
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A multicomponent sulfonylation of O-aryl oximes via iminyl radicals with the insertion of sulfur dioxide under photoredox catalysis is achieved. This multicomponent reaction of O-aryl oximes, potassium metabisulfite, alkenes, and nucleophiles under visible-light irradiation is efficient, giving rise to a range of sulfones in moderate to good yields. A broad reaction scope is presented with good functional group compatibility.
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