A P-cyclodextrin bonded stationary phase was employed for the enantioresolution of propranolol and several analogues in conjunction with various polar organic mobile phases. The effects of structural alterations in the non-polar regions of the analytes were found to exert profound changes upon chira
β-Cyclodextrin inclusive interaction driven separation of organic compounds
✍ Scribed by H. B. Ji; Q. P. Long; H. Y. Chen; X. T. Zhou; X. F. Hu
- Publisher
- American Institute of Chemical Engineers
- Year
- 2010
- Tongue
- English
- Weight
- 497 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0001-1541
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The antimalarial drug primaquine (PQ) and its contaminant, the positional isomer quinocide (QC) have been successfully separated using capillary electrophoresis with either __β__‐cyclodextrin (__β__‐CD) or 18‐crown‐6 ether (18C6) as chiral mobile phase additive. The interactions of the
The results of a Raman and solid state 13 C-NMR spectroscopic investigation aimed at studying the conformation of piroxicam (P) and its interaction with -cyclodextrin (CD) in 1 : 1 amorphous PCD inclusion compound are reported. The 1700 -1200 cm Ϫ1 FT-Raman and the 13 C CP/MAS NMR spectra of 1 :