Medena NoikhamTanakorn KittikoolSirilata YotphanMahidol University2019-08-232019-08-232018-06-15Synthesis (Germany). Vol.50, No.12 (2018), 2337-23461437210X003978812-s2.0-85045136757https://repository.li.mahidol.ac.th/handle/20.500.14594/45424© 2018 Georg Thieme Verlag Stuttgart New York - Synthesis. A highly efficient iodine-catalyzed oxidative cross-dehydrogenative coupling reaction of quinoxalinones and indoles has been developed. Without the requirement of peroxide and acid, this reaction utilizes a catalytic amount of molecular iodine to facilitate the C-C bond formation under ambient air. This simple and easy-to-handle protocol represents an interesting synthetic alternative with a good scope and functional group compatibility.Mahidol UniversityChemical EngineeringChemistryIodine-Catalyzed Oxidative Cross-Dehydrogenative Coupling of Quinoxalinones and Indoles: Synthesis of 3-(Indol-2-yl)quinoxalin-2-one under Mild and Ambient ConditionsArticleSCOPUS10.1055/s-0037-1609445