Abstract
Inhere, the first instance of copper-catalyzed oxidative amination of sulfenamides for the synthesis of sulfinamidines was documented. Employing air as the terminal oxidant, a variety of secondary and primary amines can be effectively transformed into their target products. This reaction boasts excellent chemoselectivity, mild conditions, straightforward operation, and broad substrate compatibility, which has significant implications for the fields of pharmaceuticals and organic synthesis.