## Abstract Separation of the two enantiomers of racemic α‐ and β‐amino acids on two ligand exchange chiral stationary phases (CSPs) prepared previously by covalently bonding sodium __N__‐((__S__)‐1‐hydroxymethy‐3‐methylbutyl)‐__N__‐undecylaminoacetate or sodium __N__‐((__R__)‐2‐hydroxy‐1‐phenyleth
New ligand exchange chiral stationary phase for the liquid chromatographic resolution of α- and β-amino acids
✍ Scribed by Myung Ho Hyun; Sang Cheol Han; Sung Hee Whangbo
- Book ID
- 108339286
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 380 KB
- Volume
- 992
- Category
- Article
- ISSN
- 1873-3778
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📜 SIMILAR VOLUMES
A liquid chromatographic ligand exchange chiral stationary phase (CSP) derived from (S)-leucinol was applied in the separation of the enantiomers of 12 beta-amino acids. The resolution was quite successful especially for the enantiomers of beta-amino acids containing aromatic functional group in the
## Liquid chromatographic direct resolution of b-amino acids on a chiral crown ether stationary phase A chiral stationary phase (CSP) prepared by bonding (+)-(18-crown-6)-2,3,11,12tetracarboxylic acid to silica gel was used for the direct resolution of b-amino acids. To determine the optimum mobil
## Abstract The liquid chromatographic enantiomer separation of __N__‐fluorenylmethoxycarbonyl (FMOC) protected α‐amino acids and their ethyl ester derivatives was performed on polysaccharide‐derived chiral stationary phases, Chiralcel OD, Chiralpak AD, and Chiralpak AS. In general, Chiralcel OD an