Rh(III)-Catalyzed Controlled Ortho-Amidation of Arylamides with Dioxazolones Using Weakly Coordinating Native Primary Amide as the Directing Group

Abstract

Herein, we report a controlled introduction of an amide unit at the ortho-position of an electron-deficient arylamide system without affording any cyclized products using user-friendly dioxazolone as an amidating reagent in the presence of a Rh(III)catalyst. This is the first report where native primary amide has been utilized as a weakly coordinating group for site-selective C−N bond formation reaction. The developed protocol works under external auxiliary-free conditions with a wide substrate scope.