Publication | Closed Access
Generation of Cation Radicals from Enamines and Their Reactions with Olefins
92
Citations
6
References
1992
Year
Enantioselective SynthesisEngineeringAlkene MetathesisBiochemistryCeiv CompoundsNatural SciencesRadical (Chemistry)Organic ChemistryTheir ReactionsCatalysisChemistryTetrabutylammonium CeriumAbstract Cation RadicalsAsymmetric CatalysisSynthetic ChemistryCation RadicalsBiomolecular Engineering
Abstract Cation radicals of enamines, generated by the oxidation with CeIV compounds, react with electron-rich olefins to give the addition products. The formal α-alkylation of formylacetate is realized by the reaction of 3-(1-pyrrolidinyl)propenoate and olefins by the use of tetrabutylammonium cerium(IV) nitrate as an oxidant.
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