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Diastereo- and enantioselective construction of cyclohexanone-fused spirospyrazolones containing four consecutive stereocenters through asymmetric sequential reactions
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Citations
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References
2016
Year
EngineeringDiphenylprolinol Silyl EtherNatural SciencesDiversity-oriented SynthesisConsecutive StereocentersCyclohexanone-fused SpirospyrazolonesAsymmetric Sequential ReactionsSequential OxidationOrganic ChemistryCatalysisStereoselective SynthesisChemistryPharmacologyAsymmetric CatalysisSynthetic ChemistryEnantioselective Synthesis
The diastereo- and enantioselective synthesis of cyclohexanone-fused spirospyrazolones through an asymmetric Michael/Michael/aldol cascade reaction catalyzed by squaramide and diphenylprolinol silyl ether, followed by a sequential oxidation was developed.
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