Enantiomeric separation by MEKC using dodecyl thioglycoside surfactants: Importance of an equatorially oriented hydroxy group at C-2 position in separation of dansylated amino acids

Electrophoresis

Volumn 30, Issue 15, 2009, Pages 2743-2746

  Tano, Chiharu ^a   Son, Sang Hyun ^a   Furukawa, Jun Ichi ^a   Furuike, Tetsuya ^b   Sakairi, Nobuo ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b KANSAI UNIVERSITY   (Japan)

Author keywords

Alkyl thioglycosides; Chiral surfactants; Enantiomeric separation; Micellar electrokinetic chromatography

Indexed keywords

AMINO ACIDS; ENANTIOMERS; HYDROPHOBICITY; LIQUID CHROMATOGRAPHY; MICELLES; SULFUR COMPOUNDS;

ALKYL THIOGLYCOSIDE; AMINO-ACIDS; ANALYTES; C-2 POSITIONS; CHIRAL SURFACTANT; DODECYL THIOGLYCOSIDES; ENANTIOMERIC SEPARATION; HYDROXY GROUPS; MICELLAR ELECTROKINETIC CHROMATOGRAPHY; THIOGLYCOSIDES;

SURFACE ACTIVE AGENTS;

GALACTOSE; GLUCOPYRANOSIDE; GLUCOSE; MANNOSE; METHYL MANNOSIDE; SURFACTANT; THIOGLYCOSIDE; 1 MYRISTOYL 2 (12 ((5 DIMETHYLAMINO 1 NAPHTHALENESULFONYL)AMINO)DODECANOYL) SN GLYCERO 3 PHOSPHOCHOLINE; 1-MYRISTOYL-2-(12-((5-DIMETHYLAMINO-1-NAPHTHALENESULFONYL)AMINO)DODECANOYL)-SN-GLYCERO-3-PHOSPHOCHOLINE; AMINO ACID; PHOSPHATIDYLCHOLINE;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; CONTROLLED STUDY; ENANTIOMER; HYDROPHILICITY; HYDROPHOBICITY; MICELLAR ELECTROKINETIC CHROMATOGRAPHY; MICELLE; SEPARATION TECHNIQUE; CHEMISTRY; ISOLATION AND PURIFICATION; METHODOLOGY; STEREOISOMERISM;

AMINO ACIDS; CHROMATOGRAPHY, MICELLAR ELECTROKINETIC CAPILLARY; GALACTOSE; GLUCOSE; HYDROPHOBICITY; MICELLES; PHOSPHATIDYLCHOLINES; STEREOISOMERISM; SURFACE-ACTIVE AGENTS; THIOGLYCOSIDES;

EID: 70350769342     PISSN: 01730835     EISSN: 15222683     Source Type: Journal    
DOI: 10.1002/elps.200800685     Document Type: Article

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