Liquid chromatographic enantioseparation of beta-blocking agents with (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isothiocyanate as chiral derivatizing agent

Citation
M. Peter et al., Liquid chromatographic enantioseparation of beta-blocking agents with (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isothiocyanate as chiral derivatizing agent, J CHROMAT A, 910(2), 2001, pp. 247-253
Citations number
36
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
Volume
910
Issue
2
Year of publication
2001
Pages
247 - 253
Database
ISI
SICI code
Abstract
The applicability of (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isoth iocyanate [(R,R)-DANI] as a recently developed chiral derivatizing agent fo r the enantioseparation of a series of beta -blockers is described. The thi ourea diastereomers formed were analyzed by reversed-phase high-performance liquid chromatography, mixtures of water and methanol or acetonitrile bein g used for elution. Conditions of derivatizations (temperature, reagent exc ess and reaction time) were optimized, and the effects of organic modifiers on the retention and separation were investigated; the diastereomers could readily be baseline separated with methanol-containing mobile phases with resolutions between 1.58 and 2.72. (C) 2001 Elsevier Science B.V. All right s reserved.