Comparative LC Enantioseparation of Novel PPAR Agonists on Cellulose- and Amylose-Based Chiral Stationary Phases
β Scribed by Luca Piemontese; Salvatore Faliti; Giuseppe Carbonara; Antonio Laghezza; Paolo Tortorella; Fulvio Loiodice
- Book ID
- 111791763
- Publisher
- Springer
- Year
- 2009
- Tongue
- English
- Weight
- 767 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0009-5893
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract The direct HPLC enantiomeric separation of several ferrocenylalcohols on the commercially available Chiralcel OD and Chiralcel OJ columns has been evaluated in normalβphase mode. Almost all the compounds were resolved on one or both chiral stationary phases (CSPs) with separation factor
The chiral resolution of seven aromatase inhibitors (four triazole derivatives (Ia, Ib, Ic, and Id) and three tetrazole derivatives (IIa, IIb, and IIc)) was achieved on Chiralcel OJ-R [cellulose tris (4-methyl benzoate)], Chiralcel OD-RH [cellulose tris (3,5-dimethylphenyl carbamate)], and Chiralpak
## Abstract The discrimination ability of three celluloseβbased chiral stationary phases (CSPs) was evaluated towards the enantiomers of basic drugs, using ACN as the main solvent in polar organic mobile phases. The study was focused on CSPs containing cellulose tris(3βchloroβ4βmethylphenylcarbamat
## Abstract Two chiral stationary phases derived from derivatized amylose (Chiralpak ADβH and Chiralpak IA) have been used to separate the enantiomers of new diethyl benzamidoarylmethylphosphonates. The data obtained indicate that all the studied compounds could be easily baseline resolved on both