Enantiomers can be separated by microcolumn liquid chromatography with methylated &cyclodextrin @-CD) as a mobile phase additive. Effects of the mobile phase composition on the retention behaviour of the analytes were examined. The separation factor achieved with heptakis(2,3,6-tri-0-methyl)+-CD as
Separation of ferrocenylethanol enantiomers by microcolumn liquid chromatography with β-cyclodextrin as mobile phase additive
✍ Scribed by Toyohide Takeuchi; Tomoo Miwa
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 430 KB
- Volume
- 666
- Category
- Article
- ISSN
- 1873-3778
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Some racemic nonsteroidal anti‐inflammatory drugs, namely naproxen, indoprofen, ketoprofen, flurbiprofen, carprofen, cicloprofen, flunoxaprofen and suprofen were separated into their enantiomers by nano‐LC. Chiral recognition was achieved adding to the mobile phase heptakis (2,3,6‐tri‐_
## Abstract Dansyl derivatives of racemic phenylalanine and its analogs have been resolved by microcolumn liquid chromatography with γ‐cyclodextrin as mobile phase additive. The enantioselectivity of the system was influenced by the concentrations of both γ‐cyclodextrin and acetonitrile in the mobi
## Abstract Enantiomeric resolution of dansyl amino acids by microcolumn liquid chromatography with γ‐cyclodextrin as a mobile phase additive has been investigated. The separation factor for the enantiomers increased with increasing γ‐cyclodextrin concentration as well as with decreasing acetonitri