Enantiomeric separation of promethazine and d,l-α-amino-β-[4-(1,2-dihydro-2-oxo-quinoline)] propionic acid drugs by capillary zone electrophoresis using albumin as chiral selectors-Reference-Cited by-同舟云学术

Enantiomeric separation of promethazine and d,l-α-amino-β-[4-(1,2-dihydro-2-oxo-quinoline)] propionic acid drugs by capillary zone electrophoresis using albumin as chiral selectors

Published:1999-06 Issue:2-3 Volume:392 Page:175-181
ISSN:0003-2670
Container-title:Analytica Chimica Acta
language:en
Short-container-title:Analytica Chimica Acta

Author:

Zhang Xin-Xiang,Hong Feng,Chang Wen-Bao,Ci Yun-Xiang,Ye Yun-Hua

Publisher

Elsevier BV

Subject

Spectroscopy,Environmental Chemistry,Biochemistry,Analytical Chemistry

Reference26 articles.

1. Pharmaceuticals and related drugs

2. Chiral separations by host-guest complexation with cyclodextrin and crown ether in capillary zone electrophoresis

3. Chiral recognition and enantiomeric resolution based on host-guest complexation with crown ethers in capillary zone electrophoresis

4. Enantiomer resolution by using capillary zone electrophoresis: Resolution of racemic tryptophan and determination of the enantiomer composition of commercial pharmaceutical epinephrine

5. Improved chiral separations of basic compounds in capillary electrophoresis using .beta.-cyclodextrin and tetraalkylammonium reagents

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