Publication | Closed Access
Pig Liver Esterase-catalyzed Hydrolyses of Racemic Diacetates of Bicyclic Compounds and Interpretation of the Enantiomeric Specificity of PLE
11
Citations
8
References
1991
Year
Asymmetric CatalysisBiosynthesisAbstract PigEngineeringBiochemistryNatural SciencesBiocatalysisEnantiomeric SpecificityOrganic ChemistryBicyclic CompoundsChemistryStereoselective SynthesisPharmacologyRacemic DiacetatesActive Site ModelSynthetic ChemistryEnantioselective SynthesisNatural Product Synthesis
Abstract Pig liver esterase-catalyzed hydrolyses of racemic diacetates of bicyclic compounds, bicyclo[2.2.1]heptanes, bicyclo[2.2.2]octanes, and bicyclo[3.2.1]octanes gave the optically active monoacetates and diacetates. The enantiomeric specificity of PLE toward diacetates of racemic diol substrates was analyzed by using the active site model.
| Year | Citations | |
|---|---|---|
Page 1
Page 1