Examination of methodology for the synthesis of cyclic thioether peptide libraries derived from linear tripeptides

✍ Scribed by Kade D. Roberts; Nicholas J. Ede

• Publisher: John Wiley and Sons
• Year: 2007
• Tongue: English
• Weight: 294 KB
• Volume: 13
• Category: Article
• ISSN: 1075-2617
• DOI: 10.1002/psc.904

✦ Synopsis

Abstract

Work was undertaken to examine methodology for the cyclization of linear tripeptides on the solid phase via intramolecular S‐alkylation using the Multipin^™^ Solid‐Phase Peptide Synthesis platform. While previous work had shown that this chemistry could be used to efficiently cyclize linear tetrapeptide libraries, application of this synthetic strategy to the model linear tripeptide sequence Leu‐Ser‐Lys resulted in significant cyclic dimer formation. Ultimately, it was found that the addition of a large excess of lithium in the form of LiCl to the cyclization solution, significantly reduced cyclic dimer formation affording highly pure crude cyclic monomer. The application of this modified cyclization protocol to the preparation of cyclic peptide libraries was successfully demonstrated with the synthesis of a 20‐membered library 4{1–20} based on the linear tripeptide sequence Leu‐Xxx‐Lys in which the position Xxx was varied with the standard 20 proteogenic residues. Copyright © 2007 European Peptide Society and John Wiley & Sons, Ltd.