The couple Pro/AzaPro : A means of β-turn formation control synthesis and conformation of two AzaPro-containing dipeptides

Tetrahedron Letters

Volumn 33, Issue 36, 1992, Pages 5209-5212

  Lecoq, Alain ^a   Boussard, Guy ^a   Marraud, Michel ^a   Aubry, André ^b  

^a LAB DE CHIM PHYS MACROMOLECULAIRE   (France)

^b CNRS   (France)

Author keywords

azapeptides; Azaproline; conformational analysis; peptidomimetics; turn

Indexed keywords

AMINO ACID DERIVATIVE; AZAPROLINE DERIVATIVE; DIPEPTIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; PEPTIDE SYNTHESIS; PRIORITY JOURNAL;

EID: 0026806775     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)79134-9     Document Type: Article

References (14)

1. Peptide Backbone Modifications: a Structure-Activity Analysis of Peptides Containing Amide Bond Surrogates, Conformational Constraints, and Related Backbone Replacements
2. Analogue and Conformational Studies on Peptide Hormones and Other Biologically Active Peptides
3. Azapeptides
4. Polypeptides. Part XIII. Preparation of ?-aza-amino-acid (carbazic acid) derivatives and intermediates for the preparation of ?-aza-peptides