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