Publication | Closed Access
Process Development of the Sharpless Catalytic Asymmetric Dihydroxylation Reaction To Prepare Methyl (2<i>R</i>,3<i>S</i>)-2,3-Dihydroxy-3-phenylpropionate
32
Citations
5
References
2000
Year
EngineeringProcess DevelopmentOrganic ChemistryChemistryBiosynthesisHomogeneous CatalysisBiochemistryBiocatalysisCatalysisAsymmetric CatalysisEnantioselective SynthesisCatalytic SynthesisBiomolecular EngineeringAdh Reaction-2,3-Dihydroxy-3 PhenylpropionateNatural SciencesMajor ImpurityMolecular CatalysisSynthetic Chemistry
A typical Sharpless catalytic asymmetric dihydroxylation (ADH) process to make methyl (2R,3S)-2,3-dihydroxy-3 phenylpropionate has been successfully developed. The ADH reaction was exothermic and complete in 2−3 h without affecting the optical purity and yield. The major impurity of methyl (2R)-hydroxy-3-keto-phenylpropionate, which may seriously damage the quality of diol, has been identified and removed properly in the process.
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