Copyright (c) 2013 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Effect of Different Acids Addition on Chiral Separation of Phthalylvaline by Quinine Carbamate Based Chiral Stationary
Corresponding Author(s) : Rachid Fegas
fegasrachid@yahoo.fr
Asian Journal of Chemistry,
Vol. 25 No. 12 (2013): Vol 25 Issue 12
Abstract
The quinine carbamate type chiral stationary phase used for direct enantiomer separation of amino acid was studied. The influence of mobile phase composition, methanol and different acids were systematically investigated to gain an insight into the overall chiral recognition mechanism.
Keywords
Enantiomer separation
Chiral stationary phase
LC mobile phase composition
Phthalylvaline
Fegas, R., Zerkout, S., Taberkokt, M., Bettache, Z., & Righezza, M. (2013). Effect of Different Acids Addition on Chiral Separation of Phthalylvaline by Quinine Carbamate Based Chiral Stationary. Asian Journal of Chemistry, 25(12), 6953–6956. https://doi.org/10.14233/ajchem.2013.15319
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX