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Asymmetric Co(II)-Catalyzed Cyclopropanation with Succinimidyl Diazoacetate: General Synthesis of Chiral Cyclopropyl Carboxamides
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Citations
43
References
2009
Year
Succinimidyl DiazoacetateActive Cyclopropyl CarboxamidesEngineeringHeterocyclicEffective CatalystChiral Cyclopropyl CarboxamidesOrganic ChemistryCatalysisStereoselective SynthesisAsymmetric CoChemistryGeneral SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
[Co(P1)] is an effective catalyst for asymmetric cyclopropanation with succinimidyl diazoacetate. The Co(II)-catalyzed reaction is suitable for various olefins, providing the desired cyclopropane succinimidyl esters in high yields and excellent diastereo- and enantioselectivity. The resulting enantioenriched cyclopropane succinimidyl esters can serve as convenient synthons for the general synthesis of optically active cyclopropyl carboxamides.
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