A visible‐light‐induced method was developed to synthesize selenylated cyclic boronic esters through intermolecular oxyselenenylation. This method can be performed under additive‐free and photocatalyst‐free conditions and generates potentially pharmaceutically useful heterocycles. A plausible reaction mechanism was proposed based on several control experiments and previous reports.
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Qu et al. (2024) studied this question.
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