Comparison of the separation of aziridine isomers applying heptakis(2,3-di-O-methyl-6-sulfato)β-CD and heptakis(2,3-di-O-acetyl-6-sulfato)β-CD in aqueous and nonaqueous systems
✍ Scribed by Yaser Bitar; Björn Degel; Tanja Schirmeister; Ulrike Holzgrabe
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 204 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0173-0835
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## 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
## Abstract The characteristics of the new chiral stationary phase heptakis(2,3‐di‐__O__‐methyl‐6‐__O__‐__tert__‐butyldimethylsilyl)‐β‐cyclodextrin are outlined and compared with permethyl‐ and perethyl‐β‐cyclodextrins.