Literature DB >> 15280966

Combined approach using capillary electrophoresis and NMR spectroscopy for an understanding of enantioselective recognition mechanisms by cyclodextrins.

Bezhan Chankvetadze1.   

Abstract

This tutorial review describes the contribution of chiral capillary electrophoresis in combination with other instrumental techniques, especially nuclear magnetic resonance spectroscopy, to a better understanding of the chiral recognition mechanisms by cyclodextrins. Aspects such as affinity pattern of enantiomers towards various cyclodextrins as well as the stoichiometry of the resulting complexes, the equilibrium constants and the structure of complexes are addressed. In addition to the aforementioned techniques, the usefulness of complementary instrumental and molecular modeling techniques for an understanding of the chiral recognition mechanisms of cyclodextrins is also illustrated.

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Year:  2004        PMID: 15280966     DOI: 10.1039/b111412n

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  4 in total

1.  Chiral recognition of ephedrine: Hydrophilic polymers bearing β-cyclodextrin moieties as chiral sensitive host molecules.

Authors:  Sabrina Gingter; Helmut Ritter
Journal:  Beilstein J Org Chem       Date:  2011-11-10       Impact factor: 2.883

2.  Acylation of Chiral Alcohols: A Simple Procedure for Chiral GC Analysis.

Authors:  Mireia Oromí-Farrús; Mercè Torres; Ramon Canela
Journal:  J Anal Methods Chem       Date:  2012-05-09       Impact factor: 2.193

Review 3.  Recent applications of affinity interactions in capillary electrophoresis.

Authors:  Christian Schou; Niels H H Heegaard
Journal:  Electrophoresis       Date:  2006-01       Impact factor: 3.535

4.  Self-assembly of cyclic hexamers of γ-cyclodextrin in a metallosupramolecular framework with d-penicillamine.

Authors:  Supattra Somsri; Naoto Kuwamura; Tatsuhiro Kojima; Nobuto Yoshinari; Takumi Konno
Journal:  Chem Sci       Date:  2020-08-17       Impact factor: 9.825

  4 in total

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