Determination of enantiomeric excess for 2,3-dihydroxy-3-phenylpropionate compounds by capillary electrophoresis using hydroxypropyl-β-cyclodextrin as chiral selector
✍ Scribed by Yan Zhao; Xing-Bin Yang; Qiao-Feng Wang; Peng-Juan Nan; Ying Jin; Sheng-Yong Zhang
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 163 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0899-0042
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The single isomer, fully and permanently charged heptakis-2,3-di-. methyl-6-sulfato --cyclodextrin was used to study the complexation behavior of the enantiomers of noncharged analytes in capillary electrophoresis. Separation selectivities were calculated from the measured effective mobilities and
## Abstract The enantiomeric separation of a series of basic pharmaceuticals (β‐blockers, local anesthetics, sympathomimetics) has been investigated in nonaqueous capillary electrophoresis (NACE) systems using heptakis(2,3‐di‐__O__‐methyl‐6‐__O__‐sulfo)‐β‐cyclodextrin (HDMS‐β‐CD) in combination wit