Publication | Closed Access
Highly Enantioselective Organocatalytic Carbonyl‐Ene Reaction with Strongly Acidic, Chiral Brønsted Acids as Efficient Catalysts
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Citations
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References
2008
Year
EngineeringOrganic ChemistryChemistryMild Reaction ConditionsChemical EngineeringNovel OrganocatalystsIon-pair IntermediatesStereoselective SynthesisBiochemistryStrongly AcidicChiral Brønsted AcidsCatalysisEfficient CatalystsAsymmetric CatalysisEnantioselective SynthesisCatalytic SynthesisExcellent Ee ValuesBiomolecular EngineeringNatural SciencesSynthetic Chemistry
You can count on the counterion in ion-pair intermediates to induce high levels of asymmetry in the title reaction. The efficient transformation proceeds under mild reaction conditions in the presence of an air-stable N-triflylphosphoramide in a low catalyst loading of just 1 mol % to give substituted α-hydroxyesters in good yields and with excellent ee values (see scheme; R=aryl).
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