Publication | Closed Access
Highly efficient asymmetric reduction of arylpropionic aldehydes by Horse Liver Alcohol Dehydrogenase through dynamic kinetic resolution
61
Citations
17
References
2007
Year
EngineeringOrganic Solvent MixturesArylpropionic AldehydesOrganic ChemistryBiochemical EngineeringAlcohol DehydrogenasesAldehyde DehydrogenaseBiochemistryBiocatalysisCatalysisPharmacologyNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringDynamic Kinetic ResolutionEnantiomeric RatiosGood Reaction YieldsNatural SciencesEnzyme CatalysisSynthetic ChemistryDrug DiscoveryCarbonyl Metabolism
The enantioselective synthesis of (2S)-2-phenylpropanol and (2S)-2-(4-iso-butylphenyl)propanol ((S)-Ibuprofenol) has been achieved by means of Horse Liver Alcohol Dehydrogenase (HLADH) in buffered aqueous solution or buffered organic solvent mixtures; under the reaction conditions, a dynamic kinetic resolution (DKR) process was realized with good reaction yields and enantiomeric ratios.
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