Iron-catalyzed synthesis of substituted 3-arylquinolin-2(1 H )-ones via an intramolecular dehydrogenative coupling of amido-alcohols.
Léo BettoniNicolas JolyInès MendasMatteo Maria MoscogiuriJean-François LohierSylvain GaillardAlbert PoaterJean-Luc RenaudPublished in: Organic & biomolecular chemistry (2024)
Here we report an iron-complex-catalyzed synthesis of various mono- and di-substituted quinolin-2(1 H )-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.