## Abstract In the present study the migration order of the propranolol enantiomers with various native CDs and neutral and charged CD derivatives was examined in capillary electrophoresis (CE). The reversal of the enantiomer migration order was observed due to sulfation of β‐CD on its primary hydr
Capillary electrophoresis, nuclear magnetic resonance and mass spectrometry studies of opposite chiral recognition of chlorpheniramine enantiomers with various cyclodextrins
✍ Scribed by Bezhan Chankvetadze; Naira Burjanadze; Dieter Bergenthal; Dirk Strickmann; Prof. Dr. Gottfried Blaschke; Giorgio Pintore; Riccardo Cerri
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 610 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0173-0835
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Capillary electrophoresis (CE) allows the observation of the opposite affinities of the enantiomers of (±)-verapamil [2-isopropyl-2,8-bis(3,4-dimethoxyphenyl)-6-methyl-6-azaoctannitrile, VP] toward -cyclodextrin (-CD) and heptakis(2,3,6-tri-Omethyl)--CD (TM--CD). In addition, in the presence of
## Abstract The possible mechanisms for the chiral recognition of 2‐(__R__)‐__N__‐[1‐(6‐aminopyridin‐2‐ylmethyl)piperidin‐4‐yl]‐2‐[(1__R__)‐3,3‐difluorocyclopentyl]‐2‐hydroxy‐2‐phenylacetamide (RR‐M3), and its enantiomer (SS‐M3) with octakis(2,3‐di‐__O__‐acetyl‐6‐sulfo)‐γ‐cyclodextrin (ODAS‐γ‐CD) a