Issue 21, 2018

Alkylation–peroxidation of α-carbonyl imines or ketones catalyzed by a copper salt via radical-mediated Csp3–H functionalization

Abstract

The catalytic alkylation–peroxidation of α-carbonyl imines or ketones was enabled by a simple copper salt under very mild reaction conditions. The transformations involved radical-mediated Csp3–H functionalization and afforded stable α-amino or α-alkyloxyl peroxides in good to excellent yields. This strategy would potentially provide a straightforward approach to direct difunctionalization of carbon−heteroatom double bonds and construction of structurally novel organic peroxides.

Graphical abstract: Alkylation–peroxidation of α-carbonyl imines or ketones catalyzed by a copper salt via radical-mediated Csp3–H functionalization

Supplementary files

Article information

Article type
Research Article
Submitted
31 Jul 2018
Accepted
17 Sep 2018
First published
18 Sep 2018

Org. Chem. Front., 2018,5, 3083-3087

Alkylation–peroxidation of α-carbonyl imines or ketones catalyzed by a copper salt via radical-mediated Csp3–H functionalization

M. Lei, Y. Li, S. Cao, X. Hou and L. Gong, Org. Chem. Front., 2018, 5, 3083 DOI: 10.1039/C8QO00797G

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