Publication | Closed Access
Trapping of Trifluoromethyl Radical with Enolacetate and in situ Generated Enol
18
Citations
3
References
1988
Year
Situ Generated EnolChemical EngineeringEngineeringOrganic ElectrochemistryRadical (Chemistry)Active Methylene CompoundsTrifluoromethyl RadicalElectrosynthesisFluorous SynthesisOrganic ChemistryChemistryHalogenationAbstract ElectrochemicallyBiomolecular Engineering
Abstract Electrochemically generated trifluoromethyl radical can be trapped with enolacetates and enol generated in situ from β-ketoesters and 1,3-diketones, affording trifluoromethylated active methylene compounds.
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