Capillary electrophoretic separation of enantiomers using the single isomer heptakis-(2,3-dimethyl-6-sulfato)-β-cyclodextrin as chiral resolving agent in methanol–water background electrolytes
✍ Scribed by Hong Cai; Gyula Vigh
- Book ID
- 108341605
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 430 KB
- Volume
- 827
- Category
- Article
- ISSN
- 1873-3778
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📜 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
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