Issue 4, 2017

Diaminodiacid-based synthesis of macrocyclic peptides using 1,2,3-triazole bridges as disulfide bond mimetics

Abstract

A new approach for the efficient construction of 1,2,3-triazole bridges as disulfide surrogates in peptides, utilizing the diaminodiacid strategy was established. Two thanatin derivatives were prepared with 1,5- and 1,4-disubstituted 1,2,3-triazole diaminodiacids as building blocks. The antibacterial activity studies are also described here.

Graphical abstract: Diaminodiacid-based synthesis of macrocyclic peptides using 1,2,3-triazole bridges as disulfide bond mimetics

Supplementary files

Article information

Article type
Paper
Submitted
10 Nov 2016
Accepted
13 Dec 2016
First published
12 Jan 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 2110-2114

Diaminodiacid-based synthesis of macrocyclic peptides using 1,2,3-triazole bridges as disulfide bond mimetics

Y. Guo, C. Liu, H. Song, F. Wang, Y. Zou, Q. Wu and H. Hu, RSC Adv., 2017, 7, 2110 DOI: 10.1039/C6RA26617G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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