Gas-chromatographic enantiomer separation of proteinogenic amino acid derivatives: Comparison of Chirasil-val and Chirasil-gamma-dex used as chiral stationary phases

Citation
V. Schurig et al., Gas-chromatographic enantiomer separation of proteinogenic amino acid derivatives: Comparison of Chirasil-val and Chirasil-gamma-dex used as chiral stationary phases, ENANTIOMER, 4(3-4), 1999, pp. 297-303
Citations number
23
Categorie Soggetti
Chemistry
Journal title
ENANTIOMER
ISSN journal
10242430 → ACNP
Volume
4
Issue
3-4
Year of publication
1999
Pages
297 - 303
Database
ISI
SICI code
1024-2430(1999)4:3-4<297:GESOPA>2.0.ZU;2-S
Abstract
The polymeric chiral stationary phases (CSPs) Chirasil-Val (polysiloxane-li nked N-propanoyl-L-valine tert-butyl amide) and Chirasil-gamma-Dex (polysil oxane-linked (3-O-butanoyl-2,6-di-O-n-pentyl)-gamma-cyclodextrin) are compa red with regard to their advantages and disadvantages in the gas-chromatogr aphic enantiomer separation of proteinogenic amino acid derivatives (triflu oroacetyl or pentafluoropropanoyl amides, ethyl or 2-proyyl esters). Each C SP shows a distinct behaviour according to thermal stability and enantiosel ectivity towards the amino acid derivatives resulting in different elution orders. Some attempts are made to combine the advantages of both CSPs.