Synthesis of Aib-Pro oligopeptides by repeated azirine coupling with the Aib-Pro synthon

Helvetica Chimica Acta

Volumn 95, Issue 8, 2012, Pages 1325-1351

  Stoykova, Svetlana A ^a   Linden, Anthony ^a   Heimgartner, Heinz ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

Bend ribbon structure; 2H Azirine 3 amines; Azirine oxazolone method; Peptides

Indexed keywords

2H-AZIRINE-3-AMINES; ACTIVATING REAGENTS; AZIRINE/OXAZOLONE METHOD; BASIC CONDITIONS; COUPLING CONDITION; COUPLING REACTION; CRYSTALLINE STATE; DIPEPTIDE; METHYL ESTERS; NMR TECHNIQUES; NO ACTIVATION; OLIGOPEPTIDES; PEPTIDE SYNTHESIS; RIBBON STRUCTURES; ROOM TEMPERATURE; SYNTHONS; TETRA PEPTIDE;

AMIDES; CHEMICAL ACTIVATION; CRYSTALLINE MATERIALS; ORGANIC COMPOUNDS; PEPTIDES; SELF ASSEMBLY; X RAY CRYSTALLOGRAPHY;

CONFORMATIONS;

2 AMINO 2 METHYLPROPIONIC ACID; ANTIBIOTIC AGENT; AZIRINE DERIVATIVE; BASE; DIPEPTIDE; ESTER DERIVATIVE; HEXAPEPTIDE; OCTAPEPTIDE; OLIGOPEPTIDE; PROLINE DERIVATIVE; REAGENT; TETRAPEPTIDE;

ARTICLE; CONFORMATION; CROSS COUPLING REACTION; DRUG SYNTHESIS; HYDROLYSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PEPTIDE SYNTHESIS; PRIORITY JOURNAL; ROOM TEMPERATURE; SOLUTION AND SOLUBILITY; X RAY CRYSTALLOGRAPHY;

EID: 84865314759     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.201200136     Document Type: Article

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