Synthesis of a single-isomer sulfated β-cyclodextrin carrying nonidentical substituents at all of the C2, C3, and C6 positions and its use for the electrophoretic separation of enantiomers in acidic aqueous and methanolic background electrolytes, Part 2: Heptakis(2-O-methyl-6-O-sulfo) cyclomaltoheptaose

Electrophoresis

Volumn 26, Issue 20, 2005, Pages 3849-3860

  Busby, M Brent ^a   Vigh, Gyula ^a  

^a TEXAS A AND M UNIVERSITY   (United States)

Author keywords

Capillary electrophoresis; Enantiomer separations; Heptakis(2 O methyl 6 O sulfo) cyclomaltoheptaose; Single isomer sulfated cyclodextrin; Sulfated cyclodextrin

Indexed keywords

CYCLODEXTRINS; ENANTIOMERS;

ANALYTES; ENANTIOMERS SEPARATION; HEPTAKI(2-O-METHYL-6-O-SULFO)-CYCLOMALTOHEPTAOSE; NON-IDENTICAL; SEPARATION SELECTIVITY; SINGLE-ISOMER; SINGLE-ISOMER SULPHATED CYCLODEXTRIN; SULFATED CYCLODEXTRINS; WEAK BASIS;

CAPILLARY ELECTROPHORESIS;

AMFEBUTAMONE; ATROPINE; BETA CYCLODEXTRIN; CHLORAMPHETAMINE; CHLORPHENIRAMINE; DILTIAZEM; ELECTROLYTE; EPHEDRINE; HOMATROPINE; ISOPRENALINE; KETAMINE; KETOTIFEN; METADRENALIN; METHANOL; METHOXYPHENAMINE; NOREPHEDRINE; ORCIPRENALINE; OXEDRINE; PHENYLETHANOLAMINE; PIPEROXAN; PROPRANOLOL; SCOPOLAMINE; TERBUTALINE;

ACIDITY; AQUEOUS SOLUTION; ARTICLE; CAPILLARY ELECTROPHORESIS; CHEMICAL INTERACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; DRUG DETERMINATION; DRUG STRUCTURE; ELECTROPHORETIC MOBILITY; ENANTIOMER; ENANTIOSELECTIVITY; SEPARATION TECHNIQUE; SULFATION;

EID: 27644555681     PISSN: 01730835     EISSN: None     Source Type: Journal    
DOI: 10.1002/elps.200500191     Document Type: Article

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