A family of single-isomer, sulfated γ-cyclodextrin chiral resolving agents for capillary electrophoresis: Octa(6-O-sulfo)-γ-cyclodextrin
✍ Scribed by Wenhong Zhu; Gyula Vigh
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 155 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0173-0835
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📜 SIMILAR VOLUMES
## Abstract A novel single‐isomer positively charged β‐cyclodextrin (β‐CD), mono‐6^A^‐butylammonium‐6^A^‐deoxy‐β‐cyclodextrin tosylate (BuAM‐β‐CD), has been synthesized, characterized, and used for the enantioseparations of α‐hydroxy acids, carboxylic acids, and ampholytic analytes by capillary ele
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
The new, single-isomer, octakis 2,3-diacetyl-6-sulfato -␥-cyclodextrin Ž . ODAS-␥ CD has been used for the capillary electrophoretic separation of the enantiomers of weak acids, mostly nonsteroidal anti-inflammatory agents, in a high pH background electrolyte where all the acidic analytes were fully