𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and structure of AzAsx-Pro-containing Aza-peptides

✍ Scribed by Frédéric André; Michel Marraud; Guy Boussard; Claude Didierjean; André Aubry

Publisher
Elsevier Science
Year
1996
Tongue
French
Weight
218 KB
Volume
37
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and conformational analysis of
Synthesis and conformational analysis of AzAsx-containing oligopeptides
✍ Frédéric André; Guy Boussard; Michel Marraud; Claude Didierjean; André Aubry 📂 Article 📅 1995 🏛 Springer Netherlands 🌐 English ⚖ 233 KB

For the sake of improving synthetic methods and evaluating the conformational perturbation induced by the substitution of AzAsx for the Asx residue in the cognate dipeptide R-CO-Asx-Pro-NHR', we prepared the AzAsxdipeptide sequence by making use of the crystalline triphosgene. This reagent allows, i

Peptides containing the sulfonamide junc
Peptides containing the sulfonamide junction: Synthesis, structure, and conformation of Z-Tau-Pro-Phe-NHiPr
✍ A. Calcagni; D. Rossi; M. Paglialunga Paradisi; G. Lucente; G. Luisi; E. Gavuzzo 📂 Article 📅 1997 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 183 KB 👁 1 views

The taurine (Tau) containing tripeptide derivative Z-Tau-Pro-Phe-NHiPr (1) has been synthesized as suitable sulfonamido-pseudopeptide model to investigate formation and conformational properties of folded secondary structures stabilized by intramolecular H bonds directly involving the sulfonamide ju

X-Pro peptides: Synthesis and solution c
X-Pro peptides: Synthesis and solution conformation of benzyloxycarbonyl-(Aib-Pro)4methyl ester. Evidence for a novel helical structure
✍ Y. V. Venkatachalapathi; P. Balaram 📂 Article 📅 1981 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 427 KB

## Abstract The synthesis of the octapeptide, benzyloxycarbonyl‐(α‐aminoisobutyryl‐L‐prolyl)~4~‐methyl ester [__Z__‐(Aib‐Pro)~4~‐OMe] and an analysis of its solution conformation is reported. The octapeptide is shown to possess three strong intramolecular hydrogen bonds on the basis of studies of t