Novel method converts benzyl sulfides to sulfonyl fluorides under mild conditions, indicating enhanced synthetic utility.
Sulfonyl fluorides serve as privileged synthetic building blocks with a broad utility. The development of cost-effective and efficient synthetic routes to these motifs remains a significant challenge. Herein, we present a novel trichloroisocyanuric acid (TCCA)-mediated one-pot protocol for the efficient conversion of benzyl sulfides to sulfonyl fluorides. This transition-metal-free strategy operates under mild conditions, exhibiting exceptional operational simplicity and low cost while enabling diverse alkyl and (hetero)aryl sulfonyl fluoride construction with enhanced synthetic utility.
No takes yet. Share an insight, caveat, or question.
Fan et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: