Stereoisomeric separation of some flavanones using highly succinate-substituted α-cyclosophoro-octadecaoses as chiral additives in capillary electrophoresis

Carbohydrate Research

Volumn 346, Issue 1, 2011, Pages 133-139

  Kwon, Chanho ^a   Jung, Seunho ^a  

^a Konkuk University   (South Korea)

Author keywords

Cyclosophoro octadecaoses; Chiral capillary electrophoresis (CE); Enantioseparation; Flavanone; Flavonoid

Indexed keywords

ALKALINE TREATMENT; CHIRAL ADDITIVES; CHIRAL CAPILLARY ELECTROPHORESIS (CE); CHIRAL SEPARATIONS; ENANTIOSEPARATIONS; FLAVANONE; FLAVONOIDS; O-GLYCOSIDES; RHODOBACTER SPHAEROIDES; SUCCINOYLATION;

ADDITIVES; CAPILLARY ELECTROPHORESIS; CHIRALITY; GLUCOSE;

ELECTROCHEMISTRY;

ALPHA CYCLOSOPHORO OCTADECAOSE DERIVATIVE; ERIODICTYOL; FLAVANONE DERIVATIVE; GLYCOSIDE; HESPERETIN; HESPERIDIN; ISOSAKURANETIN; NARINGENIN; SUCCINIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CAPILLARY ELECTROPHORESIS; CHIRALITY; PRIORITY JOURNAL; STEREOISOMERISM; SYNTHESIS;

ALPHA-CYCLODEXTRINS; ELECTROPHORESIS, CAPILLARY; FLAVANONES; HYDROGEN-ION CONCENTRATION; MOLECULAR STRUCTURE; STEREOISOMERISM; SUCCINIC ACID; TEMPERATURE;

RHODOBACTER SPHAEROIDES;

EID: 78650206808     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2010.10.007     Document Type: Article

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