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Photocatalytic strategy generates alkyl radicals to form alkyl-aryl sulfides without metals, suggesting a new method.
The sulfenylation of organohalides has become a powerful strategy for CS bond formation. However, methods for activating alkyl halides in this context remain scarce. Herein, we report a simple photocatalytic strategy that generates alkyl radicals from alkyl halides via halogen atom transfer. These radicals subsequently couple efficiently with N ‐arylsulfenyl phthalimides to afford alkyl‐aryl sulfides. This approach is transition‐metal‐free, operates under mild conditions, and exhibits a broad substrate scope.
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Yang et al. (2026) studied this question.
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