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Structural rationale for the chiral separation and migration order reversal of clenpenterol enantiomers in capillary electrophoresis using two different β-cyclodextrins

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Abstract

NMR spectroscopy experiments, molecular dynamics simulations, and theoretical chemistry calculations provide insight into the structural and energetic determinants of the distinct binding of clenpenterol enantiomers to two cyclodextrins and the migration order reversal of their respective inclusion complexes in capillary electrophoresis.

Graphical abstract: Structural rationale for the chiral separation and migration order reversal of clenpenterol enantiomers in capillary electrophoresis using two different β-cyclodextrins

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Publication details

The article was received on 14 Jul 2017, accepted on 27 Sep 2017 and first published on 27 Sep 2017


Article type: Communication
DOI: 10.1039/C7CP04761D
Citation: Phys. Chem. Chem. Phys., 2017, Advance Article
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    Structural rationale for the chiral separation and migration order reversal of clenpenterol enantiomers in capillary electrophoresis using two different β-cyclodextrins

    A. Salgado, E. Tatunashvili, A. Gogolashvili, B. Chankvetadze and F. Gago, Phys. Chem. Chem. Phys., 2017, Advance Article , DOI: 10.1039/C7CP04761D

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