Organic Letters · 2019 · 71 citations · 51 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisRetrosynthetic AnalysisBuilding Block MethodologyDirect SynthesisFused Heterocycle SynthesisKetonesMulticomponent Heterocycle SynthesisOne-pot Heterocycle SynthesisQuinoline ChemistryQuinoline Synthesis
The first synthesis of 2,3-diaroyl quinolines via a formal [3 + 2 + 1] cycloaddition of enaminones, aryl methyl ketones, and aryl amines is disclosed. This reaction efficiently affords a 1,4-dicarbonyl scaffold, which is a useful building block for constructing complex fused heterocycles. Furthermore, the 1,4-dicarbonyl scaffold has been used directly to prepare pyridazino[4,5- b]quinoline skeletons in one-pot.
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