Effect of Different Acids Addition on Chiral Separation of Phthalylvaline by Quinine Carbamate Based Chiral Stationary | Health & Environmental Research Online (HERO)

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Citation
Tags

HERO ID

7450542

Reference Type

Journal Article

Title

Effect of Different Acids Addition on Chiral Separation of Phthalylvaline by Quinine Carbamate Based Chiral Stationary

Author(s)

Fegas, R; Zerkout, S; Taberkokt, M; Bettache, Z; Righezza, M

Year

2013

Is Peer Reviewed?

Yes

Journal

Asian Journal of Chemistry
ISSN: 0970-7077
EISSN: 0975-427X

Publisher

Chemical Publishing Co.

Volume

Issue

Page Numbers

6953-6956

Language

English

DOI

10.14233/ajchem.2013.15319

Web of Science Id

WOS:000325088800103

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. Â© 2013 Asian Journal of Chemistry.

Keywords

Enantiomer separation; Chiral stationary phase; LC mobile phase composition; Phthalylvaline