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Asymmetric Michael Addition Induced by the Anion of an Imidazolium Salt
18
Citations
21
References
2012
Year
Catalytic EntityEngineeringBiochemistryImidazolium SaltNatural SciencesOrganic ChemistryCatalysisCatalytic Michael AdditionChemistryAsymmetric Michael AdditionAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringIon Structure
Abstract We describe the application of a chiral catalytic imidazolium salt derived from trans ‐ L ‐hydroxyproline, the anion being the catalytic entity, as a catalyst for the asymmetric Michael addition. We report the first example of a catalytic Michael addition using this type of catalyst, leading to excellent yields (up to 99 %) and good selectivities (up to 99:1 dr , up to 82 % ee ).
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