Indirect separation of chiral proteinogenic α-amino acids using the florescence active (1R,2R)-N- [(2-isothiocyanato)cyclohexyl]-6-methoxy-4-quinolinylamide) as chiral derivatizing agent. A comparison

Journal of Chromatography A

Volumn 795, Issue 2, 1998, Pages 251-261

  Kleidernigg, O P ^a   Lindner, W ^a,b  

^a UNIVERSITY OF GRAZ   (Austria)

^b UNIVERSITY OF VIENNA   (Austria)

Author keywords

Amino acids; Derivatization, electrophoresis; Derivatization, LC; Diastereomer separation; Enantiomer separation

Indexed keywords

ALPHA AMINO ACID; FLUORESCENT DYE; N [(2 ISOTHIOCYANATO)CYCLOHEXYL] 6 METHOXY 4 QUINOLINYLAMIDE; UNCLASSIFIED DRUG;

AMINO ACID ANALYSIS; ARTICLE; CAPILLARY CHROMATOGRAPHY; CONTROLLED STUDY; DERIVATIZATION; DIASTEREOISOMER; ENANTIOMER; FLUORESCENCE ANALYSIS; INTERMETHOD COMPARISON; LASER; LIQUID CHROMATOGRAPHY; PH; PRIORITY JOURNAL; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; STEREOCHEMISTRY; TEMPERATURE SENSITIVITY;

EID: 0032488935     PISSN: 00219673     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0021-9673(97)00869-8     Document Type: Article

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