Comparative HPLC enantioseparation of ferrocenylalcohols on two cellulose-based chiral stationary phases
✍ Scribed by Angela Patti; Sonia Pedotti; Claudia Sanfilippo
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 327 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0899-0042
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The direct HPLC enantiomeric separation of several ferrocenylalcohols on the commercially available Chiralcel OD and Chiralcel OJ columns has been evaluated in normal‐phase mode. Almost all the compounds were resolved on one or both chiral stationary phases (CSPs) with separation factor (α) ranging from 1.06 to 2.88 while the resolution (R~s~) varied from 0.63 to 12.70 In the separation of the α‐ferrocenylalcohols 1a–e and the phenyl analogues 2a–e, which were all resolved except 1c, a similar trend in the retention behavior for the two series of alcohols was evidenced and the selectivity was roughly complementary on the two investigated CSP. For three ferrocenylacohols, chosen as model compounds, the influence of the mobile phase composition and temperature on the enantioseparation were investigated and additional information on the chiral recognition mechanism were deduced from the chromatographic behavior of their acetylderivatives. Chirality, 2007. © 2007 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract Retention and enantioseparation behavior of ten 2,2′‐disubstituted or 2,3,2′‐trisubstituted 1,1′‐binaphthyls and 8,3′‐disubstituted 1,2′‐binaphthyls, which are used as catalysts in asymmetric synthesis, was investigated on eight chiral stationary phases (CSPs) based on β‐CD, polysacchar
Four cellulose mixed 10-undecenoate/carbamate derivatives, simultaneously bearing 10-undecenoyl and variously substituted phenylaminocarbonyl groups, were chemically bonded on allylsilica gel. The study of the effect of these substitutions on the performance of the resulting chiral supports, and a c
## Abstract Composite chiral stationary phases (CSPs) were prepared on the basis of cellulose derivatives coated or bonded onto silica. “Molecular exterior” type CSPs were prepared by mixing together two different cellulose tris‐derivatives before or after being coated or bonded onto silica, and th
## Abstract Phenylcarbonate, benzoylformate, and __p__‐toluenesulfonylcarbamate of cellulose and five new benzoylcarbamate derivatives of both cellulose and amylose were synthesized and their chiral recognition abilities were evaluated as chiral stationary phases (CSPs) for high‐performance liquid