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Volumn 345, Issue 16, 2010, Pages 2408-2412
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Carboxymethylated cyclosophoraose as a novel chiral additive for the stereoisomeric separation of some flavonoids by capillary electrophoresis
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Author keywords
Carboxymethylated cyclosophoraoses; Chiral capillary electrophoresis; Flavonoids; Stereoisomeric separation
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Indexed keywords
CARBOXYMETHYLATED CYCLOSOPHORAOSES;
CHIRAL ADDITIVES;
CHIRAL CAPILLARY ELECTROPHORESIS;
CHIRAL SELECTOR;
FLAVONOIDS;
MIGRATION TIME;
NARINGIN;
STEREOISOMERIC SEPARATION;
BLOOD VESSELS;
CAPILLARY ELECTROPHORESIS;
CHEMICAL MODIFICATION;
ELECTROCHEMISTRY;
PHENOLS;
PH EFFECTS;
AURANTIIN;
CARBOXYMETHYLATED CYCLOSOPHORAOSE;
CATECHIN, 3,5,7,3',4' PENTAHYDROXYFLAVANONE;
ERIODICTYOL;
FLAVONOID;
GLUCAN;
HESPERETIN;
HESPERIDIN;
ISOSAKURANETIN;
NARINGENIN;
UNCLASSIFIED DRUG;
ARTICLE;
CAPILLARY ELECTROPHORESIS;
CHEMICAL STRUCTURE;
PH;
PRIORITY JOURNAL;
RHIZOBIUM TRIFOLII;
STEREOISOMERISM;
TEMPERATURE;
ELECTROPHORESIS, CAPILLARY;
FLAVONOIDS;
GLUCANS;
HYDROGEN-ION CONCENTRATION;
MOLECULAR STRUCTURE;
STEREOISOMERISM;
TEMPERATURE;
RHIZOBIUM LEGUMINOSARUM;
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EID: 77958098194
PISSN: 00086215
EISSN: None
Source Type: Journal
DOI: 10.1016/j.carres.2010.08.009 Document Type: Article |
Times cited : (25)
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References (24)
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