Iodide promotes oxidative synthesis of sulfilimines from sulfenamides and phenols, suggesting new pathways.
Iodide-promoted oxidative S-arylation of sulfenamides with phenols is described for the synthesis of sulfilimines without the use of a transition-metal catalyst. Using TBAI and CHP, this iodide-promoted oxidative reaction affords aryl sulfilimines in variable yields. Control experiments are consistent with radical involvement and indicate that a free phenolic hydroxyl group is important for productive coupling under the standard conditions.
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Zhu et al. (2026) studied this question.
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