Structure-enantioselectivity relationships for the study of chiral recognition in peptide enantiomer separation on cinchona alkaloid-based chiral stationary phases by HPLC: Influence of the N-terminal protecting group

Journal of Separation Science

Volumn 26, Issue 17, 2003, Pages 1499-1508

  Czerwenka, Christoph ^a   Lämmerhofer, Michael ^a   Lindner, Wolfgang ^a  

^a Institute of Analytical Chemistry   (Austria)

Author keywords

Chiral anion exchanges; Chiral recognition; Enantiomer separation; Peptides; Protecting groups

Indexed keywords

AMINO ACIDS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ION EXCHANGE; PHASE COMPOSITION;

ENANTIOSELECTIVITY; MOBILE PHASES;

POLYPEPTIDES;

AMINO ACID; ANION; CINCHONA ALKALOID; PEPTIDE;

AMINO TERMINAL SEQUENCE; ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; COMPARATIVE STUDY; CONTROLLED STUDY; DERIVATIZATION; ENANTIOMER; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PHASE SEPARATION; PRIORITY JOURNAL; PROTECTION; SEPARATION TECHNIQUE;

CINCHONA;

EID: 0344898837     PISSN: 16159306     EISSN: None     Source Type: Journal    
DOI: 10.1002/jssc.200301577     Document Type: Article

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