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Noncovalent Organocatalysis: A Powerful Tool for the Nucleophilic Epoxidation of α-Ylideneoxindoles
91
Citations
47
References
2011
Year
EngineeringOrganic ChemistryNovel OrganocatalystsRedox ChemistryStereoselective SynthesisSpiro Compoundsα-Ylideneoxindole EstersBiochemistryBiocatalysisPowerful ToolCatalysisPharmacologyAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringComplex H-bond NetworkNatural SciencesNoncovalent OrganocatalysisNucleophilic Epoxidation
A novel asymmetric nucleophilic epoxidation for α-ylideneoxindole esters has been successfully devised, resulting in enantioenriched spiro compounds with two new contiguous stereocenters. The employed (S)-α,α-diphenylprolinol functions as a bifunctional catalyst, creating a complex H-bond network in conjunction with a substrate and an oxidant.
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