Affiliation:
1. Graduate School of Pharmaceutical Sciences Kyoto University Sakyo-ku, Kyoto 606-8501 Japan
Abstract
AbstractSulfilimines and their derivatives have garnered considerable interest in both synthetic and medicinal chemistry. Photochemical nitrene transfer to sulfides is known as a conventional synthetic approach to sulfilimines. However, the existing methods have a limited substrate scope stemming from the incompatibility of singlet nitrene intermediates with nucleophilic functional groups. Herein, we report the synthesis of N‐sulfonyl sulfilimines via visible‐light‐mediated energy transfer to sulfonyl azides, uncovering the previously overlooked reactivity of triplet nitrenes with sulfides. This reaction features broad functional group tolerance, water compatibility, and amenability to the late‐stage functionalization of drugs. Thus, this work represents an important example of energy transfer chemistry that overcomes challenges in traditional synthetic methods.
Funder
Japan Society for the Promotion of Science
Japan Agency for Medical Research and Development