Publication | Closed Access
Construction of Quaternary Stereocenters by Efficient and Practical Conjugate Additions to α,β‐Unsaturated Ketones with a Chiral Organic Catalyst
207
Citations
19
References
2005
Year
Chemical EngineeringEngineeringAll-carbon Quaternary StereocenterPractical Conjugate AdditionsCatalytic SynthesisChiral Organic CatalystOrganic ChemistryQuaternary StereocentersCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringAdded Value
Added value: The conjugate addition of cyclic or acyclic α-substituted β-ketoesters to α,β-unsaturated ketones using a chiral organic catalyst (1) can be achieved with good enantioselectivity, diastereoselectivity, and yield. This asymmetric CC bond formation strategy provides a range of chiral building blocks 2 that contain an all-carbon quaternary stereocenter.
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