Enantioselective Intramolecular Decarboxylative C−H Bond Func‐tionalization of Quinazolinones with Amino Acids by Visible Light Photoredox Catalysis

Abstract

AbstractThe direct visible light‐mediated intramolecular decarboxylative C−H functionalization of Csp2−H bond adjacent to the nitrogen of a heteroarene has been achieved by iridium‐catalyzed photodecarboxylative radical cyclization. This method offers rapid entry to the synthesis of quinazolinone scaffolds from easily accessible starting materials. The newly developed protocol is mild, operationally simple, oxidant free and general. The utility of this unique Csp3−Csp2 bond forming reaction has been demonstrated in the syntheses of Circumdatin, Sclerotigenine and Benzomalvin A class of quinazolinone natural products and their congeners. The present work represents an interesting example of use of memory of chirality in decarboxylative C−C bond forming enantioselective photoredox reaction.