## Abstract A chiral stationary phase (CSP) based on (–)‐(18‐crown‐6)‐2,3,11,12‐tetracarboxylic acid was evaluated for the direct resolution of the enantiomers of dipeptides and tripeptides. The type and concentration of the acid and the methanol content were optimized with regard to retention time
✦ LIBER ✦
High-Performance liquid chromatographic separation of enantiomers of unusual amino acids possessing cycloalkane or cycloalkene skeletons on a chiral crown ether containing stationary phase
✍ Scribed by G. Török; A. Péter; F. Fülöp
- Publisher
- Springer
- Year
- 1998
- Tongue
- English
- Weight
- 540 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0009-5893
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## Abstract A doubly tethered chiral stationary phase (CSP) containing N–CH~3~ amide linkage based on (+)‐(18‐crown‐6)‐2,3,11,12‐tetracarboxylic acid was applied to the resolution of various β‐amino acids. The chiral recognition behaviors for the resolution of β‐amino acids on the doubly tethered C