High-performance liquid chromatography chiral recognition

Franco, P., Senso, A., Minguillon, C., and Oliveros, L. (1998) 3,5-Dimethylphenylcarbamates of amylose, chitosan and cellulose bonded on silica gel. Comparison of their chiral recognition abilities as high-performance liquid chromatography chiral stationary phases, J. Chromatogr. A 796, 265-272. 

Hyun, M.H., Ryoo, J.J., and Pirkle, W.H., Experimental support differentiating two proposed chiral recognition models for the resolution of N- 3,5-dinitrobenzoyl)-alpha-arylalkylamines on high-performance liquid chromatography chiral stationary phases, J. Chromatogr. A, 886,47, 2000. 

In another study, the authors reported a comparative study of the enantiomeric resolution of miconazole and the other two chiral drugs by high performance liquid chromatography on various cellulose chiral columns in the normal phase mode [79], The chiral resolution of the three drugs on the columns containing different cellulose derivatives namely Chiralcel OD, OJ, OB, OK, OC, and OE in normal phase mode was described. The mobile phase used was hexane-isopropanol-diethylamine (425 74 1). The flow rates of the mobile phase used were 0.5, 1, and 1.5 mL/min. The values of the separation factor (a) of the resolved enantiomers of econazole, miconazole, and sulconazole on chiral phases were ranged from 1.07 to 2.5 while the values of resolution factors (Rs) varied from 0.17 to 3.9. The chiral recognition mechanisms between the analytes and the chiral selectors are discussed. 

Anionic Catalysis Several bulky methacrylates afford highly isotactic, optically active polymers having a single-handed helical structure by asymmetric polymerization. The effective polymerization mechanism is mainly anionic but free-radical catalysis can also lead to helix-sense-selective polymerization. The anionic initiator systems can also be applied for the polymerization of bulky acrylates and acrylamides. The one-handed helical polymethacrylates show an excellent chiral recognition ability when used as a chiral stationary phase for high-performance liquid chromatography (HPLC) [97,98]. 

Hui, F. (2004) High Performance Liquid Chromatography and Capillary Electrophoresis Chiral Recognition Mechanisms Using Glycopeptide Macrocyclic Antibiotics as Selectors, Fenxi Huaxue 32, 964-968. 

Poly(TrMA) exhibits chiral recognition ability toward various types of racemic compounds when used as a chiral stationary phase for high-performance liquid chromatography (HPLC).14-16... 

Chromatography is one of the most important methods for direct studies of molecular and chiral recognition by CyDs. Today it has split into several branches, e.g. gas chromatography, GC, high-performance liquid chromatography, HPLC, and capillary electrophoresis and other electromigration techniques, that enable us not only to detect the recognition but also to estimate the complex stoichiometry and formation constant and, consequently, the enthalpies and entropies of complex for-... 

Shen J, Liua S, Li P, Shen X, Okamoto Y (2012) Controlled synthesis and chiral recognition of immobilized cellulose and amylose tris(cyclohexylcarbamate)s/3-(triethoxysilyl)propylcarbamates as chiral packing materials for high-performance liquid chromatography. J Chromatogr A 1246 137-144... 

Despite the long recognition of chirality in POPs, it has only been fairly recently that studies of chiral POPs have been possible, after the introduction of analytical technology for stereoisomer separation by enantioselective gas chromatography (GC), high performance liquid... 

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