Ergot alkaloids as novel chiral selectors in capillary electrophoresis
✍ Scribed by Ingelse, Benno A. ;Reijenga, Jetse C. ;Claessens, Henk A. ;Everaerts, Frans ;Flieger, Mirko
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 231 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0935-6304
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📜 SIMILAR VOLUMES
Lambda-carrageenan, a linear high molecular weight sulfated polysaccharide, has been employed as a chiral selector in capillary electrophoresis for the separation of enantiomers of weakly basic pharmaceutical compounds. The racemic compounds that were enantioresolved included propranolol, pindolol,
## Abstract New single‐isomer, cationic β‐cyclodextrins, including mono‐6‐deoxy‐6‐pyrrolidine‐β‐cyclodextrin chloride (pyCDCl), mono‐6‐deoxy‐6‐(__N__‐methyl‐pyrrolidine)‐β‐cyclodextrin chloride (__N__‐CH~3~‐pyCDCl), mono‐6‐deoxy‐6‐(__N__‐(2‐hydroxyethyl)‐pyrrolidine)‐β‐cyclodextrin chloride (__N__‐
## Abstract A novel chiral selector, clindamycin succinate, was synthesized and first used as a chiral selector in capillary electrophoresis (CE). The chiral resolution ability of this kind of clindamycin derivation was studied by CE using some racemic drugs as model analytes. From the experimental