Issue 36, 2015

Oxidative α,ω-diyne coupling as an approach towards novel peptidic macrocycles

Abstract

The Glaser–Hay diyne coupling proved to be an efficient cyclisation approach towards diyne containing peptidic macrocycles. A variety of tetrapeptide-based macrocyclic 1,3-diynes were obtained from O-propargylated serine or tyrosine residues using Cu(OAc)2·H2O and NiCl2 under an O2-atmosphere. The effect of the linear 1,3-diyne on peptide conformations was studied by NMR and compared with a macrocycle bearing a saturated linker.

Graphical abstract: Oxidative α,ω-diyne coupling as an approach towards novel peptidic macrocycles

Supplementary files

Article information

Article type
Paper
Submitted
08 Jun 2015
Accepted
20 Jul 2015
First published
06 Aug 2015

Org. Biomol. Chem., 2015,13, 9398-9404

Author version available

Oxidative α,ω-diyne coupling as an approach towards novel peptidic macrocycles

S. Verlinden, N. Geudens, J. C. Martins, D. Tourwé, S. Ballet and G. Verniest, Org. Biomol. Chem., 2015, 13, 9398 DOI: 10.1039/C5OB01153A

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