Enantiomers, liquid chromatographic

Ceccato, A., Boulanger, B., Chiap, P., Hubert, P., Crommen, J. (1998). Simultaneous determination of methylphenobarbital enantiomers and Phenobarbital in human plasma by online coupling of an achiral precolumn to a chiral liquid chromatographic column. J. Chromatogr. A 819, 143-153. 

Clark, B.J., Hamdi, A., Berrisford, R.G., Sahanathan, S., Meams, AJ. (1991). Reversed-phase and chiral high-performance liquid chromatographic assay of hupivacaine and its enantiomers in clinical samples after continuous extraplural infusion. J. Chromatogr. 553,383-390. 

Corlett, S.A., Chrystyn, H. (1996). High-Performance liquid chromatographic determination of the enantiomers of cyclophosamide in semm. J. Chromatogr. B 682, 337-342. 

Gimenez, F., Farinotti, R., Thuillier, A., Hazebroucq, G., Wainer, I.W. (1990). Determination of the enantiomers of mefloquine in plasma and whole blood using a coupled achiral-chiral high-performance liquid chromatographic system. J. Chromatogr. 529, 339-346. 

Hutta, M., Rybar, I., Chalanyova, M. (2002). Liquid chromatographic method development for determination of fungicide enantiomers by achiral and chiral column switching technique in water and soil. J. Chromatogr. A 959, 143-152. 

Masurel, D., Wainer, I.W. (1989). Analytical and preparative high-performance liquid chromatographic separation of the enantiomers of isofamide, cyclophoshamide, and trofosfa-mide and their determination in plasma. J. Chromatogr 490, 133-143. 

Rojkovicova, T., Lehotay, J., Cizmarik, J. (2003h). Kinetic study of derivatives of phenylcar-hamic acid enantiomers in rabbit blood serum using an online coupled column liquid chromatographic system. Pharmazie 58, 483-486. 

Soltes, L., Sebille, B. (1997). Reversible binding interactions between the tryptophan enantiomers and albumins of different animal species as determined by novel high performance liquid chromatographic methods an attempt to localize the d- and L-tryptophan binding sites on the human serum albumin polypeptide chain by using protein fragments. Chirality 9, 373-379. 

High-pressure liquid chromatographic (HPLC) analysis performed with a chiral mobile phase (57,58) confirmed in all the conglomerate systems that the S inhibitors are selectively occluded only in the bulk of the S substrate crystals, typically in amounts of 0.5-1% (and, by symmetry, occlusion of R occurs only in R crystals). The selective adsorption causes, furthermore, a drastic decrease in the growth (and possibly nucleation) rate of the affected enantiomer, leading to efficient kinetic resolution various conglomerate systems have been resolved by this method (54). 

Liquid Chromatographic Enantiomer Separation and Chiral Recognition... 

Some other cinchona alkaloid derivatives that have been synthesized and were evaluated as chiral selectors for liquid chromatographic enantiomer separation comprise CSPs based on cinchonan hydrazides [68], cinchonan ureas [42], cin-chonan amides [42], and urea-linked cinchonan-calixarene hybrid selectors [42]... 

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