Publication | Closed Access
Transition-Metal-Free C-3 Arylation of Quinoline-4-ones with Arylhydrazines
69
Citations
60
References
2015
Year
Aryl Radical SourceDiversity Oriented SynthesisTransition-metal-free C-3 ArylationTransition-metal-free C-3-arylationEngineeringCross-coupling ReactionOrganic ChemistryOrganometallic CatalysisCatalysisChemistrySynthetic ChemistryQuinoline-quinolone Hybrid
A transition-metal-free C-3-arylation of quinolin-4-ones in the presence of base has been achieved by using arylhydrazines as aryl radical source and air as oxidant. The reaction proceeds smoothly at room temperature and does not require any prefunctionalization and N-protection of quinoline-4-ones. The utility of this methodology is further demonstrated in synthesis of quinoline-quinolone hybrid as well as 6-aryl-benzofuro[3,2-c]quinoline scaffold.
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