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Physical Sciences and Mathematics Commons

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Missouri University of Science and Technology

Series

1996

Enantiomer separation

Articles 1 - 2 of 2

Full-Text Articles in Physical Sciences and Mathematics

Investigation On Enantiomeric Separations Of Fluorenylmethoxycarbonyl Amino Acids And Peptides By High-Performance Liquid Chromatography Using Native Cyclodextrins As Chiral Stationary Phases, Y. Tang, J. Zukowski, Daniel W. Armstrong Sep 1996

Investigation On Enantiomeric Separations Of Fluorenylmethoxycarbonyl Amino Acids And Peptides By High-Performance Liquid Chromatography Using Native Cyclodextrins As Chiral Stationary Phases, Y. Tang, J. Zukowski, Daniel W. Armstrong

Chemistry Faculty Research & Creative Works

A systematic study was carried out to investigate enantiomeric separations of fluorenylmethoxycarbonyl (FMOC) amino acids and their peptides. Twenty amino acids were derivatized by 9-fluorenylmethyl chloroformate (FMOC-Cl) and its analogues, FMOC-glycyl-Cl and FMOC-β-alanyl-Cl. All derivatives were chromatographed on native β- and γ-cyclodextrin columns using acetonitrile as the main mobile phase component. The results indicated that glycyl and β-alanyl groups between FMOC and amino acid moieties enhanced chiral selectivities of amino acid derivatives. The addition of modifiers, triethylamine, acetic acid and methanol, into the mobile phase caused alterations in retention, enantiorecognition and elution order. The structures of amino acids and the …


Facile Liquid Chromatographic Enantioresolution Of Native Amino Acids And Peptides Using A Teicoplanin Chiral Stationary Phase, Alain Berthod, Youbang Liu, Christina Bagwill, Daniel W. Armstrong Apr 1996

Facile Liquid Chromatographic Enantioresolution Of Native Amino Acids And Peptides Using A Teicoplanin Chiral Stationary Phase, Alain Berthod, Youbang Liu, Christina Bagwill, Daniel W. Armstrong

Chemistry Faculty Research & Creative Works

The glycopeptide antibiotic teicoplanin is shown to be a highly effective stationary phase chiral selector for the resolution of underivatized amino-acid and imino-acid enantiomers. Fifty four of these compounds (including all chiral protein amino acids) as well as a number of dipeptides were resolved. Hydro-organic mobile phases are used and no buffers or added salts are needed in most cases. Hence the purified analytes are easily isolated in pure form, if needed, by evaporating of the solvent. The effect of pH, organic modifier type and amount are discussed. The enantioselective separation mechanism is examined using both molecular modeling and retention …