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Volumn 22, Issue 15, 2001, Pages 3178-3184
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Mechanistic study on the opposite migration order of clenbuterol enantiomers in capillary electrophoresis with β-cyclodextrin and single-isomer heptakis(2,3-diacetyl-6-sulfo)-β-cyclodextrin
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Author keywords
Capillary electrophoresis; Chiral recognition mechanisms; Cyclodextrins; Enantioseparations; NMR spectrometry; One dimensional ROESY
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Indexed keywords
CYCLODEXTRINS;
ENANTIOMERS;
NUCLEAR MAGNETIC RESONANCE;
SPECTROMETRY;
CHIRAL RECOGNITION MECHANISMS;
CLENBUTEROL;
DIACETYL;
ENANTIOSEPARATIONS;
MECHANISTIC STUDIES;
NMR SPECTROMETRY;
ONE-DIMENSIONAL;
ONE-DIMENSIONAL ROESY;
SINGLE-ISOMER;
Β-CD;
CAPILLARY ELECTROPHORESIS;
BETA CYCLODEXTRIN;
BETA CYCLODEXTRIN DERIVATIVE;
CLENBUTEROL;
HEPTAKIS(2,3 DIACETYL 6 SULFO) BETA CYCLODEXTRIN;
UNCLASSIFIED DRUG;
ARTICLE;
BINDING AFFINITY;
CAPILLARY ELECTROPHORESIS;
CHEMICAL STRUCTURE;
COMPLEX FORMATION;
CONTROLLED STUDY;
DRUG BINDING;
ELECTROPHORETIC MOBILITY;
ENANTIOMER;
ISOMER;
NUCLEAR OVERHAUSER EFFECT;
PROTON NUCLEAR MAGNETIC RESONANCE;
SPECTROMETRY;
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EID: 0034795481
PISSN: 01730835
EISSN: None
Source Type: Journal
DOI: 10.1002/1522-2683(200109)22:15<3178::AID-ELPS3178>3.0.CO;2-F Document Type: Article |
Times cited : (43)
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References (51)
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