Highly chemoselective homologative assembly of the α-substituted methylsulfinamide motif from N-sulfinylamines

Chem Commun (Camb). 2023 Sep 14;59(74):11065-11068. doi: 10.1039/d3cc03326k.

Abstract

α-Substituted methylsulfinamide are prepared through the homologation of electrophilic N-sulfinylamines with Li-CHXY reagents. The transformation takes place under full chemocontrol and exhibits good flexibility for preparing both N-aryl and N-alkyl analogues. Various sensitive functionalities can be accommodated on the starting materials, thus documenting a wide reaction scope.