Molecular modeling study of the recognition mechanism and enantioseparation of 4-hydroxypropranolol by capillary electrophoresis using carboxymethyl-β-cyclodextrin as the chiral selector

The Analyst ◽  
2014 ◽  
Vol 139 (16) ◽  
pp. 3901-3910 ◽  
Author(s):  
Clebio Soares Nascimento ◽  
Juliana Fedoce Lopes ◽  
Luciana Guimarães ◽  
Keyller Bastos Borges

Elution order elucidation of 4-hydroxypropranolol by capillary electrophoresis and theoretical methods.

2020 ◽  
Vol 44 (3) ◽  
pp. 958-972 ◽  
Author(s):  
Yu Zhao ◽  
Jinlong Wang ◽  
Yanru Liu ◽  
Zhen Jiang ◽  
Yongbo Song ◽  
...  

In this study, carboxymethyl-6-(4-methoxybenzylamino)-β-cyclodextrin (CMCDPN) was synthesized for the first time and managed to be used as a chiral selector to enantioseparate 13 kinds of chiral drugs by capillary electrophoresis.


The Analyst ◽  
2020 ◽  
Vol 145 (3) ◽  
pp. 1025-1032 ◽  
Author(s):  
Hui Xu ◽  
Zijie Feng ◽  
Yingxiang Du

Ionic liquid MSI-LA was used as the sole chiral selector, both cation and anion contribute in forming interactions with enantiomers.


2019 ◽  
Vol 40 (15) ◽  
pp. 1897-1903 ◽  
Author(s):  
Zoltán-István Szabó ◽  
Róbert Ludmerczki ◽  
Béla Fiser ◽  
Béla Noszál ◽  
Gergő Tóth

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