The study of enantioselectivity of all regioisomers of mono-carboxymethyl- β-cyclodextrin used as chiral selectors in CE

Journal of Separation Science

Volumn 36, Issue 7, 2013, Pages 1270-1274

  Navrátilová, Klára ^a   Řezanka, Pavel ^a   Řezanka, Michal ^b,c   Sýkora, David ^a   Jindřich, Jindřich ^c   Král, Vladimír ^a  

^a INSTITUTE OF CHEMICAL TECHNOLOGY   (Czech Republic)

^b TECHNICAL UNIVERSITY OF LIBEREC   (Czech Republic)

^c CHARLES UNIVERSITY   (Czech Republic)

Author keywords

CE; Chiral separation; Enantioselectivity; Monosubstituted carboxymethyl cyclodextrin; Regioisomer

Indexed keywords

CARBOXYMETHYL; CARBOXYMETHYL GROUP; CHIRAL COMPOUNDS; CHIRAL SEPARATIONS; DEGREE OF SUBSTITUTION; ENANTIOSEPARATIONS; PHOSPHATE BUFFERS; REGIOISOMERS;

CERIUM; CHIRALITY; MUSCULOSKELETAL SYSTEM;

ENANTIOSELECTIVITY;

BACLOFEN; BASE; BETA CYCLODEXTRIN DERIVATIVE; CARBOXYMETHYL BETA CYCLODEXTRIN; ESTER; MEFLOQUINE; MONOCARBOXYMETHYL BETA CYCLODEXTRIN; TROGER BASE; TRYPTOPHAN METHYL ESTER; UNCLASSIFIED DRUG;

ARTICLE; CAPILLARY ELECTROPHORESIS; CHIRALITY; CONTROLLED STUDY; DRUG STRUCTURE; ENANTIOMER; ENANTIOSELECTIVITY; ISOMER; MOLECULAR WEIGHT; PH; PRIORITY JOURNAL; RACEMIC MIXTURE; SYNTHESIS;

EID: 84876101868     PISSN: 16159306     EISSN: 16159314     Source Type: Journal    
DOI: 10.1002/jssc.201201144     Document Type: Article

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