Issue 91, 2018

Ruthenium-catalyzed C–H oxygenation of quinones by weak O-coordination for potent trypanocidal agents

Abstract

Ruthenium-catalysis enabled the C-5 selective C–H oxygenation of naphthoquinones, and also sets the stage for the site-selective introduction of a hydroxyl group into anthraquinones. A-ring modified naphthoquinoidal compounds represent an important class of bioactive quinones for which the present study encompasses the first C–H oxygenation strategy by weak O-coordination.

Graphical abstract: Ruthenium-catalyzed C–H oxygenation of quinones by weak O-coordination for potent trypanocidal agents

Supplementary files

Article information

Article type
Communication
Submitted
18 Sep 2018
Accepted
16 Oct 2018
First published
16 Oct 2018
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2018,54, 12840-12843

Ruthenium-catalyzed C–H oxygenation of quinones by weak O-coordination for potent trypanocidal agents

G. G. Dias, T. Rogge, R. Kuniyil, C. Jacob, R. F. S. Menna-Barreto, E. N. da Silva Júnior and L. Ackermann, Chem. Commun., 2018, 54, 12840 DOI: 10.1039/C8CC07572G

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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