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- W2039345986 abstract "The use of cyclodextrin based stationary phases was investigated for the enantiomeric separation of 20 unusual amino acids. Mobile phase, pH effects, and flow rate were optimized for each separation. Separations were limited to aqueous mobile phases. Nineteen of the amino acids were separated, with seven having a resolution ≥1.5. The highest selectivities came from the alpha, acetylated beta, and 2,6-dinitrophenyl-4-trifluoromethylphenyl derivitized beta-cyclodextrin stationary phases. Amino acids containing a 1,2,3,4 tetrahydroisoquinoline carboxylic acid structure showed great compatibility with the acetylated beta-cyclodextrin. Tyrosine analogues, due to lack of retention, were not well suited to the cyclodextrin stationary phases." @default.
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- W2039345986 date "2007-11-01" @default.
- W2039345986 modified "2023-10-16" @default.
- W2039345986 title "LC Enantiomeric Separation of Unusual Amino Acids Using Cyclodextrin‐based Stationary Phases" @default.
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- W2039345986 doi "https://doi.org/10.1080/10826070701738886" @default.
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