Abstract
The aromatic (C−H) sulfenylation reaction with S-acetamidomethyl cysteine sulfoxide (Cys(Acm)(O)) can be Trp- or Tyr-selective under acidic conditions. The red chloride anion team kicks the Cys(Acm)(O) ball into the Trp goal, whereas the blue trimethylsilyl team kicks the ball into the Tyr goal. The proton scoreline in the stands supports both teams. More information can be found in the Research Article by A. Otaka and co-workers (DOI: 10.1002/chem.202300799).
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