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• W1993824941 abstract "A highly water-soluble new cyclodextrin (CD) derivative 2-O-acetonyl-2-O-hydroxypropyl-beta-CD (2-AHP-beta-CD) was synthesized and tested as an effective chiral selector for the capillary zone electrophoretic resolution (Rs) of several basic and acidic analytes. The primary purpose of the research was to explore the capability of the 2-AHP-beta-CD as chiral selectors on comparison with the neutral CDs such as beta-CD, DM-beta-CD and HP-beta-CD. Substitution with 2-O-acetonyl-2-O-hydroxypropyl group at the secondary hydroxyl sites of the CD is aimed at influencing the magnitude and selectivity of analyte-CD interactions. The chiral resolution was strongly influenced by the concentration of the CDs and buffer pH. 2-AHP-beta-CD showed the best enantiomer resolution properties among the tested compounds, while the other CDs showed inferior or no performances at all." @default.
• W1993824941 created "2016-06-24" @default.
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• W1993824941 date "2004-12-01" @default.
• W1993824941 modified "2023-09-26" @default.
• W1993824941 title "Evaluation of newly synthesized derivative of cyclodextrin for the capillary electrophoretic separation" @default.
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• W1993824941 doi "https://doi.org/10.1016/j.chroma.2004.10.046" @default.
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