Publication | Closed Access
Resolution of Optical Isomers by Thin‐Layer Chromatography Enantiomeric Purity of D‐Penicillamine
39
Citations
25
References
1986
Year
EngineeringOrganic ChemistryOptical IsomersChemistryOptical PropertiesAnalytical ChemistryLiquid ChromatographyStereoselective SynthesisChromatographyChemical MeasurementDiversity-oriented SynthesisChromatographic AnalysisPharmacologyAsymmetric CatalysisEnantioselective SynthesisMedicineAbstract PenicillamineL‐ 3Drug Analysis
Abstract Penicillamine (1) is condensed with formaldehyde to form the enantiomeric 5,5‐dimethylthiazolidinecarboxylic acids D‐ 3 and L‐ 3 . These enantiomers are separated by TLC on CHIRALPLATE®.
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