Transport of Amino Acids Methyl Esters by a Bicyclic Crown Ether
✍ Scribed by Stephan Janus; Khalil Kraïmi; Etienne Sonveaux
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 224 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0037-9646
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✦ Synopsis
Abstract
Racemic protonated amino acid methyl esters were efficiently transported through a dichloromethane phase using L,L‐Cbz‐bis(15‐crown‐5)DOPA‐OMe as a carrier. The enantioselectivity was however marginal. The (15‐crown‐5) rings of the carrier were essential for affinity, as Cbz‐bis(12‐crown‐4)DOPA‐OMe was not a good host.
📜 SIMILAR VOLUMES
A chiral liquid chromatographic method was validated to analyze the Dand L-enantiomers of five amino acids contained in a commercial solution: aspartic acid, leucine, lysine, phenylalanine, and valine. These 10 compounds were separated on a chiral crown ether column with a mobile phase composed of w
## 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