𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of a new class of imidazole-based cyclic peptides

✍ Scribed by Gebhard Haberhauer; Frank Rominger


Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
184 KB
Volume
43
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


A new class of cyclic peptides based on dipeptidyl imidazoles is presented. Their structure consists of imidazole units alternating with standard amino acid residues and resembles naturally occurring marine cyclopeptides such as westiellamide and ascidiacyclamide.


πŸ“œ SIMILAR VOLUMES


Efficient synthesis of thioether-based c
✍ Kade D. Roberts; John N. Lambert; Nicholas J. Ede; Andrew M. Bray πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 244 KB

A new method for the synthesis of cychc peptide libraries has been developed where the key cyclisation step involves reaction between a C-terminal cysteine side chain and an N-terminal bromoacyl group. We report conditions whereby liberation of peptides from the solid support and cyclisation occur c

Synthesis of cyclic peptides and peptide
✍ Werner Tegge; Wilfried Bautsch; Ronald Frank πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 261 KB

## Abstract A new cysteine‐based disulfide linker for Fmoc solid phase peptide synthesis was developed (Fmoc‐Cys(3‐mercapto‐3‐methylbutanoic acid)OPp) that allows the on‐resin assembly and side chain deprotection of cyclic peptides. Model peptides and a cyclic peptide library of the structure [a‐a‐