The Journal of Organic Chemistry · 2020 · 26 citations · 53 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistryOrganometallic ChemistryCatalyst PreparationHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisOrganometallic SynthesisAmide Bond FormationC - H Bond FunctionalizationFunctional Group AnalysisHeterocycle FunctionalizationMild Reaction ConditionsNitrogen HeterocyclesQuinoline ChemistryQuinoline Synthesis
A cobalt(III)-catalyzed C-8 selective C–H amidation of quinoline N-oxide using dioxazolone as an amidating reagent under mild conditions is disclosed. The reaction proceeds efficiently with excellent functional group compatibility. The utility of the current method is demonstrated by gram scale synthesis of C-8 amide quinoline N-oxide and by converting this amidated product into functionalized quinolines. Furthermore, the developed catalytic method is also applicable for C-7 amidation of N-pyrimidylindolines and ortho-amidation of benzamides.
53
Yoonsu Park, Kyung Tae Park, Jeung Gon Kim et al. · Journal of the American Chemical Society · 2015 · 429 citations
Heejun Hwang, Jinwoo Kim, Jisu Jeong et al. · Journal of the American Chemical Society · 2014 · 334 citations