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Organocatalytic enantioselective desymmetrization of cyclic enonesviaphosphine promoted [3+2] annulations
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Citations
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References
2010
Year
HeterocyclicStereogenic CentresEnantioselectivity LevelsExcellent Stereochemical ControlOrganic ChemistryOrganocatalytic Enantioselective DesymmetrizationStereoselective SynthesisChemistryPharmacologyAsymmetric CatalysisEnantioselective Synthesis
Phosphine catalyzed enantioselective [3+2] cyclizations on 4-substituted 2,6-diarylidenecyclohexanones and 2,4-diarylidene-bicyclo[3.1.0]hexan-3-ones take place with high diastereo- and enantioselectivity levels. The process affords spirocyclic compounds with excellent stereochemical control of up to five stereogenic centres.
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