## Abstract Cyclopentyl and (±)‐__exo__‐2‐norbornylcarbamates of cellulose and amylose were prepared and their chiral recognition abilities as chiral stationary phases for high‐performance liquid chromatography (HPLC) were evaluated. Among these carbamates, cellulose tris(cyclopentylcarbamate) and
Reversed-phase liquid chromatographic enantioseparation by cycloalkylcarboxylates of cellulose and amylose
✍ Scribed by Takateru Kubota; Chiyo Yamamoto; Yoshio Okamoto
- Book ID
- 102075780
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 119 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0899-0042
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Three novel cycloalkylcarboxylates, cyclopentyl, cyclohexyl, and 1‐adamantylcarboxylates of cellulose and amylose were prepared and their chiral recognition abilities as chiral stationary phases (CSPs) for high‐performance liquid chromatography (HPLC) were evaluated using a methanol–water mobile phase. Among these esters, cellulose tris(cyclohexylcarboxylate) showed a relatively high chiral recognition ability. The 1‐adamantylcarboxylates of cellulose and amylose showed dissimilar chiral recognition abilities from the other two, probably due to the low degree of substitution and the high hydrophobicity of this group. Chirality 16:309–313, 2004. © 2004 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## 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