Evaluation of an optically active crown ether for the chiral separation of di- and tripeptides

Journal of Chromatography A

Volumn 716, Issue 1-2, 1995, Pages 371-379

  Kuhn, Reinhard ^a   Riester, Daniel ^a   Fleckenstein, Burkhard ^b   Wiesmüller, Karl Heinz ^b  

^a Fachhochschule Reutlingen   (Germany)

^b UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; CROWN ETHER DERIVATIVE;

COMPLEX FORMATION; CONFERENCE PAPER; DRUG PURIFICATION; ENANTIOMER; METHODOLOGY; PEPTIDE ANALYSIS; PRIORITY JOURNAL; ZONE ELECTROPHORESIS;

AMINO ACID SEQUENCE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DIPEPTIDES; ETHERS, CYCLIC; HYDROGEN-ION CONCENTRATION; INDICATORS AND REAGENTS; MOLECULAR SEQUENCE DATA; OLIGOPEPTIDES; OPTICAL ROTATION; STEREOISOMERISM;

EID: 0028841985     PISSN: 00219673     EISSN: None     Source Type: Journal    
DOI: 10.1016/0021-9673(95)00371-S     Document Type: Article

References (23)

1. Liquid Chromatographic Resolution of Enantiomeric Dipeptides on the Chiral Stationary Phase Derived from (S)-1-(6,7-Dimethyl-1-naphthyl)isobutylamine
2. Enantiomeric resolution of underivatized small peptides by HPLC with a chiral crown ether stationary phase