## Abstract The separation of R,Rβ, S,Sβ, and mesoβKoga bases on derivatized amylose chiral stationary phases (CSP) has been studied using different alcohol and alcoholβhexane mixtures as eluant. Straightβchain and branched alcohols with carbon numbers from one to four were investigated. The carbon
Enantiomeric LC separation of calcium antagonists on protein-based chiral stationary phases
β Scribed by Dr. Ersilia De Lorenzi; Anthony F. Fell; Alan L. Holmes; Gabriele Caccialanza; Gabriella Massolini; Carlo Gandini; Mikes Kitsos; Carolina Ponci
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 343 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0899-0042
No coin nor oath required. For personal study only.
β¦ Synopsis
Three chiral calcium antagonist drugs, bepridil and two dihydropyridine derivatives (nicardipine and REC 15123751, have been successfully separated within short retention times using either the a,-acid glycoprotein chiral stationary phase (Chiral AGP) or the ovomucoid column (Ultron ES-OW). Aqueous buffer at defined pH is modified by the addition of an organic component (propan-2-01, acetonitrile, ethanol) in order to modulate the retention properties of each system. The influence of pH and percentage of organic modifier on retention, selectivity, resolution, and column performance are discussed for bepridil analyzed on Chiral AGP and for the two dihydropyridines (nicardipine and REC 1512375) analyzed on Ultron E S -O W stationary phases.
π SIMILAR VOLUMES
A series of enantiomeric amides have been chromatographed on three amylose-based chiral stationary phases (CSPs): amylose tris(3,5-dimethylphenylcarbamate) (AD-CSP), amylose tris(S-phenylethylcarbamate) (AS-CSP), and amylose tris(Rphenylethyl-carbamate) (AR-CSP). The relative retentions and enantios
A direct, isocratic high-performance liquid chromatographic (HPLC) method is described for the enantiomeric separation of racemic cathinone and one of its metabolites, (+I-)-norephedrine, on a protein-based chiral stationary phase (CSP), cellobiohydrolase, known as CBH-I, under reversed-phase condit
Several benzodiazepines were enantioresolved on a new carbohydrate chiral stationary phase based on maltooligosaccharides. The role of organic modifier, ionic strength, pH and temperature are examined and the results are discussed. In general, selectivity and retention were found to decrease with in