Organic Letters · 2013 · 245 citations · 47 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryCatalyst PreparationHeterocycle SynthesisMetal CatalysisMetal OxidesOrganic SynthesisRetrosynthetic AnalysisC-h Bond ActivationCopper-catalyzed CouplingCopper-catalyzed OxidationQuinoline ChemistryQuinoline Synthesis
An efficient and concise one-pot protocol to synthesize sulfonylated quinoline N-oxides via copper-catalyzed C-H bond activation has been developed. Commercially available and less expensive aryl sulfonyl chlorides were used as the sulfonylation reagents. Various 2-aryl sulfonyl quinolines were obtained in up to 91% yields in chemo- and regioselective manners.
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