Enantioseparation of chiral N-imidazole derivatives by electrokinetic chromatography using highly sulfated cyclodextrins: Mechanism of enantioselective recognition

Electrophoresis

Volumn 26, Issue 20, 2005, Pages 3824-3832

  Danel, Cécile ^a   Lipka, Emmanuelle ^a   Bonte, Jean Paul ^a   Goossens, Jean François ^a   Vaccher, Claude ^a   Foulon, Catherine ^a  

^a UNIV LILLE   (France)

Author keywords

Aromatase inhibitor; Binding constant; Chiral electrokinetic chromatography; Highly sulfated cyclodextrins; Hydrophobicity; Inclusion; Thermodynamic parameters

Indexed keywords

CYCLODEXTRINS; ELECTRODYNAMICS; ENANTIOSELECTIVITY; HYDROPHOBICITY; LIQUID CHROMATOGRAPHY;

ANALYTES; AROMATASE INHIBITORS; BINDING CONSTANT; CHIRAL ELECTROKINETIC CHROMATOGRAPHY; CHIRAL SELECTOR; ELECTROKINETIC CHROMATOGRAPHY; ENANTIOSEPARATIONS; HIGHLY SULPHATED CYCLODEXTRIN; SULFATED CYCLODEXTRINS; THERMODYNAMIC PARAMETER;

ENANTIOMERS;

2 BENZOXAZOLONE DERIVATIVE; ALPHA CYCLODEXTRIN; BENZOTHIAZOLINONE DERIVATIVE; BETA CYCLODEXTRIN; CYCLODEXTRIN; IMIDAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; CONTROLLED STUDY; DRUG DETERMINATION; DRUG STRUCTURE; ENANTIOMER; ENANTIOSELECTIVITY; MICELLAR ELECTROKINETIC CHROMATOGRAPHY; MOLECULAR INTERACTION; MOLECULAR RECOGNITION; PH; SEPARATION TECHNIQUE; SULFATION; THERMODYNAMICS;

EID: 27644539385     PISSN: 01730835     EISSN: None     Source Type: Journal    
DOI: 10.1002/elps.200500078     Document Type: Article

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