Publication | Closed Access
Direct chromatographic separation of 2‐arylpropionic acid enantiomers using tris(3,5‐dimethylphenylcarbamate)s of cellulose and amylose as chiral stationary phases
66
Citations
16
References
1989
Year
Pharmaceutical ScienceBioorganic ChemistrySupercritical Fluid ChromatographyAnilide DerivativeOrganic ChemistryPeptide ScienceChemistryPharmaceutical ChemistryMedicinal ChemistrySeparation ScienceAnalytical ChemistryLiquid ChromatographyChromatographyDerivativesBiochemistryAcid EnantiomersDirect Chromatographic SeparationAntimicrobial CompoundChromatographic AnalysisPharmacologyEnantioselective SynthesisBiomolecular EngineeringNatural SciencesChiral Stationary PhasesTiaprofenic AcidMedicineDrug DiscoveryDrug Analysis
Abstract Direct optical resolution of antiinflammatory drugs such as ibuprofen, ketoprofen, flurbiprofen, and tiaprofenic acid were attempted by high‐performance liquid chromatography using tris(3,5‐dimethylphenylcarbamate)s of cellulose and amylose as chiral stationary phases. Although ibuprofen was not sufficiently resolved, the other three 2‐arylpropionic acids were completely resolved by amylose tris(3,5‐dimethylphenylcarbamate). Ibuprofen was resolved as anilide derivative.
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