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Highly Diastereoselective and Enantioselective Synthesis of α‐Hydroxy β‐Amino Acid Derivatives: Lewis Base Catalyzed Hydrosilylation of α‐Acetoxy β‐Enamino Esters
114
Citations
65
References
2011
Year
Asymmetric CatalysisEngineeringBiochemistryNatural SciencesDiversity-oriented Synthesisα‐Hydroxy β‐Amino AcidWide RangeOrganic ChemistryCatalytic Asymmetric HydrosilylationCatalysisChemistryHighly Diastereoselectiveα‐Acetoxy β‐Enamino Estersα-Acetoxy-β-enamino Esters 1Synthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
By design: A series of α-acetoxy-β-enamino esters 1 were synthesized and then subjected to catalytic asymmetric hydrosilylation. In the presence of a chiral Lewis base catalyst, the reactions proceeded smoothly to provide a wide range of chiral α-acetoxy β-amino acid derivatives in high yields with good diastereoselectivities and enantioselectivities.
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