Iron-catalyzed synthesis of substituted 3-arylquinolin-2(1 H)-ones via an intramolecular dehydrogenative coupling of amido-alcohols

Org Biomol Chem. 2024 Aug 28;22(34):6933-6940. doi: 10.1039/d4ob00649f.

Abstract

Here we report an iron-complex-catalyzed synthesis of various mono- and di-substituted quinolin-2(1H)-ones achieved via the intramolecular acceptorless dehydrogenative cyclization of amido-alcohols. This approach for the synthesis of N-heterocycles has provided access to underdescribed disubstituted quinolinones and represents an alternative to the well-known palladium-catalyzed coupling reactions.