Publication | Closed Access
An Efficient Asymmetric Biomimetic Transamination of α-Keto Esters to Chiral α-Amino Esters
48
Citations
84
References
2012
Year
Quinine DerivativesBioorganic ChemistryDerivativesBiochemistryEngineeringNatural SciencesEnantioselective SynthesisDiversity-oriented SynthesisOrganic ChemistryHigh YieldStereoselective Synthesisα-Keto EstersAsymmetric CatalysisSynthetic ChemistryChiral α-Amino EstersBiomolecular EngineeringChiral Bases
An efficient asymmetric biomimetic transamination of α-keto esters with quinine derivatives as chiral bases was described. A wide variety of α-amino esters containing various functional groups can be synthesized in high yield and enantioselectivity.
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