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