The Journal of Organic Chemistry · 2021 · 30 citations · 41 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistryHeterocycle SynthesisOrganic SynthesisRadical ReactionsCopper-catalyzed CouplingImidazole ChemistryImidazole SynthesisSubstrate ScopeSubstrate Scope ExpansionSubstrate Scope ProfilingSubstrate Scope Screening
We reported herein a copper-catalyzed trifluoromethylarylated cycloaddition of imidazoles and olefins using CF3SO2Cl as the radical source to synthesize highly functionalized tricyclic imidazoles. This procedure exhibits a wide range of substrate scope with 25%–93% isolated yields (36 examples). Mechanistic studies were carried out to support a free trifluoromethyl radical pathway.
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