Issue 44, 2015

Synthesis and antimicrobial activity of binaphthyl-based, functionalized oxazole and thiazole peptidomimetics

Abstract

Thirty two new binaphthyl-based, functionalized oxazole and thiazole peptidomimetics and over thirty five novel leucine-containing intermediate oxazoles and thiazoles were prepared in this study. This includes the first examples of the direct C-5 arylation of an amino acid dipeptide-derived oxazole. Moderate to excellent antibacterial activity was observed for all new compounds across Gram positive isolates with MICs ranging from 1–16 μg mL−1. Results for Gram negative E. coli and A. baumannii were more variable, but MICs as low as 4 μg mL−1 were returned for two examples. Significantly, the in vitro results with a fluoromethyl-oxazole derivative collectively represent the best obtained to date for a member of our binaphthyl peptide antimicrobials.

Graphical abstract: Synthesis and antimicrobial activity of binaphthyl-based, functionalized oxazole and thiazole peptidomimetics

Supplementary files

Article information

Article type
Paper
Submitted
06 Aug 2015
Accepted
03 Sep 2015
First published
03 Sep 2015

Org. Biomol. Chem., 2015,13, 10813-10824

Author version available

Synthesis and antimicrobial activity of binaphthyl-based, functionalized oxazole and thiazole peptidomimetics

S. M. Wales, K. A. Hammer, K. Somphol, I. Kemker, D. C. Schröder, A. J. Tague, Z. Brkic, A. M. King, D. Lyras, T. V. Riley, J. B. Bremner, P. A. Keller and S. G. Pyne, Org. Biomol. Chem., 2015, 13, 10813 DOI: 10.1039/C5OB01638J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements