This method demonstrates efficient fluorination of sulfenamides, suggesting new routes for sulfondiimidoyl fluorides and derivatives.
Despite the significant applications of sulfondiimidoyl fluorides in medicinal chemistry, efficient methods for preparing these valuable fluorinated structures remain limited. Herein, we disclose a straightforward method for the modular synthesis of symmetric and unsymmetric sulfondiimidoyl fluorides through sequential amination and oxidation of sulfinimidoyl fluoride at room temperature. The resulting sulfondiimidoyl fluorides could be converted into a diverse array of sulfondiimines, sulfondiimidate esters, and sulfondiimidamides by SuFEx reaction. Moreover, a first proof of concept for an asymmetric protocol by employing a quinidine derivative catalyst is reported.
No takes yet. Share an insight, caveat, or question.
Dong et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: