| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1387951 | Carbohydrate Research | 2010 | 5 Pages |
Abstract
A carboxymethylated cyclosophoraose (CM-Cys) was synthesized by the chemical modification of neutral Cys, which was isolated from Rhizobium trifolii TA-1. CM-Cys was successfully applied as a novel chiral selector for the separation of some flavonoids including catechin, 3,5,7,3â²,4â²-pentahydroxyflavanone, hesperidin, hesperetin, isosakuranetin, naringenin, naringin, and eriodictyol. The effects of pH, chiral additive concentration, and temperature on resolution and migration time were also studied.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yukyoung Jeon, Chanho Kwon, Eunae Cho, Seunho Jung,