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Palladium‐Catalyzed Regioselective C–H Bond <i>ortho</i>‐Acetoxylation of Arylpyrimidines
55
Citations
64
References
2010
Year
Chemical EngineeringFunctional Group ToleranceEngineeringOxygenated ArylpyrimidinesHigh RegioselectivityOrganic ChemistryOrganometallic CatalysisCatalysisChemistryAsymmetric Catalysis
Abstract An efficient and regioselective palladium‐catalyzed ortho C–H acetoxylation reaction was developed to afford ortho monoacetoxylated arylpyrimidines in good to excellent yields by using cupric trifluoroacetate as a cocatalyst. A wide variety of oxygenated arylpyrimidines were prepared with high regioselectivity and functional group tolerance.
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