Issue 6, 2019

Synthesis and biological evaluation of fluorinated analogues of ripostatin A

Abstract

Several monocyclic derivatives of 14,14′-difluororipostatin A were prepared using a catalytic Mukaiyama aldol reaction, a ring-closing metathesis reaction and a late stage click reaction as key steps. The biological activity of the produced compounds was assessed in vivo using a panel of pathogenic microorganisms. Moderate antibiotic activity was observed for 11-OMe-ripostatin A and 11-OMe-14,14′-difluororipostatin A.

Graphical abstract: Synthesis and biological evaluation of fluorinated analogues of ripostatin A

Supplementary files

Article information

Article type
Communication
Submitted
19 Nov 2018
Accepted
10 Dec 2018
First published
10 Dec 2018

Org. Biomol. Chem., 2019,17, 1362-1364

Synthesis and biological evaluation of fluorinated analogues of ripostatin A

V. Shenderman and E. V. Prusov, Org. Biomol. Chem., 2019, 17, 1362 DOI: 10.1039/C8OB02890G

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