Publication | Open Access
Copper-catalyzed olefinic C–H difluoroacetylation of enamides
99
Citations
40
References
2014
Year
Broad Substrate ScopeEngineeringEfficient Radical-free MethodFluorous SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisChemistryCopper-catalyzed Olefinic DifluoroacetylationHalogenationBiomolecular Engineering
Copper-catalyzed olefinic difluoroacetylation of enamides via direct C-H bond functionalization using BrCF2CO2Et is reported for the first time. It constitutes an efficient radical-free method for the regioselective synthesis of β-difluoroester substituted enamides which exhibits broad substrate scope, and thus demonstrates its potent application in a late stage fluorination strategy.
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