Publication | Closed Access
Copper-Catalyzed <i>N</i>-Arylation of Azoles and Mannich-Type Coupling of Ketones and Azoles under Metal-Free Conditions
38
Citations
42
References
2016
Year
Chemical EngineeringMetal-free ConditionsEngineeringCross-coupling ReactionNatural SciencesActivated AzolesDiversity-oriented SynthesisNew ProcessMannich-type CouplingOrganic ChemistryOrganometallic CatalysisCatalysisMolecular CatalysisChemistryHeterocycle ChemistryFive-membered HeterocyclesBiomolecular Engineering
A new process has been developed for the copper-catalyzed direct N-arylation of five-membered heterocycles with azoles. Five-membered heterocycles bearing an acetyl group also underwent a Mannich-type reaction with activated azoles to give the corresponding β-amino ketones under metal-free conditions. These reactions exhibited wide substrate scope, high functional group tolerance, and ease of operation, making them useful tools with numerous potential applications in synthetic chemistry.
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