Liquid chromatographic-mass spectrometric separation of oligoalanine peptide stereoisomers: Influence of absolute configuration on enantioselectivity and two-dimensional separation of diastereomers and enantiomers

Journal of Chromatography A

Volumn 1038, Issue 1-2, 2004, Pages 85-95

  Czerwenka, Christoph ^a   Maier, Norbert M ^a   Lindner, Wolfgang ^a  

^a UNIVERSITY OF VIENNA   (Austria)

Author keywords

Configuration; Diastereomers; Enantiomer separation; Peptides; Two dimensional liquid chromatography mass spectrometry

Indexed keywords

DERIVATIVES; ISOMERS; MASS SPECTROMETRY; SEPARATION; STEREOCHEMISTRY;

CHIRAL STATIONARY PHASES (CSP); ENANTIOSELECTIVITY; MOLECULAR RECOGNITION; STEREOSELECTIVITY;

LIQUID CHROMATOGRAPHY;

ALANINE; CINCHONA ALKALOID; DIPEPTIDE; TETRAPEPTIDE; TRIPEPTIDE;

AMINO TERMINAL SEQUENCE; ARTICLE; CHIRALITY; DIASTEREOISOMER; ELUTION; ENANTIOMER; ENANTIOSELECTIVITY; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; MOLECULAR MECHANICS; MOLECULAR RECOGNITION; PHASE SEPARATION; PRIORITY JOURNAL; STEREOISOMERISM;

ALANINE; CHROMATOGRAPHY, LIQUID; MASS SPECTROMETRY; STEREOISOMERISM;

CINCHONA;

EID: 2442693145     PISSN: 00219673     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chroma.2004.03.013     Document Type: Article

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