Determination of enantiomer compositions of propranolol enantiomers by chiral ionic liquid as a chiral selector and the UV-assisted spectrophotometric method

2012 ◽  
Vol 4 (8) ◽  
pp. 2283 ◽  
Author(s):  
Ghodratollah Absalan ◽  
Yousef Alipour ◽  
Zahra Rezaei ◽  
Morteza Akhond
2009 ◽  
Vol 30 (16) ◽  
pp. 2820-2828 ◽  
Author(s):  
Bin Wang ◽  
Jun He ◽  
Victoria Bianchi ◽  
Shahab A. Shamsi

2013 ◽  
Vol 5 (20) ◽  
pp. 5792 ◽  
Author(s):  
Levent Pelit ◽  
Süleyman Koçak ◽  
Füsun Okçu Pelit ◽  
Hayati Türkmen ◽  
F. Nil Ertaş

2006 ◽  
Vol 39 (7) ◽  
pp. 1439-1449 ◽  
Author(s):  
L. M. Yuan ◽  
Y. Han ◽  
Y. Zhou ◽  
X. Meng ◽  
Z. Y. Li ◽  
...  

Author(s):  
Xiaofei Ma ◽  
Jingtang Li ◽  
Xiaoqi Li ◽  
Zijie Feng ◽  
Xuan Yang ◽  
...  

Abstract Nowadays, ionic liquids (ILs) functionalized cyclodextrins (CDs) have drawn increasing attention in chiral separation. Herein, a novel β-CD derivative functionalized by L-histidinium IL, mono-6-deoxy-6-L-histidinium-β-cyclodextrin chloride (L-HMCDCl), was synthesized for the first time and utilized for enantioseparation of nefopam and chlorphenamine in capillary electrophoresis. The L-HMCDCl exhibited superior enantioselectivity compared with native β-CD. The effect of some key parameters such as chiral selector concentration, buffer pH and applied voltage on the enantioseparation was investigated in detail. In the interest of the chiral discrimination mechanism and the enhanced enantioselectivity of L-HMCDCl, molecular modeling with AutoDock was employed to study the interaction, which was in good agreement with experimental results.


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