Issue 1, 2018

A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls

Abstract

A 2-pyridone ring is a frequently occurring subunit in natural products, biologically active compounds, and pharmaceutical targets. Thus, the selective synthesis of substituted 2-pyridone derivatives through decoration and/or formation of pyridone rings has been one of the important longstanding subjects in organic synthetic chemistry. This minireview focuses on recent advances in site-selective C–H functionalization on 2-pyridone. The reported procedures are categorized according to the site selectivity that is achieved, and the substrate scope, limitations, mechanism, and controlling factors are briefly summarized.

Graphical abstract: A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls

Article information

Article type
Minireview
Submitted
18 अक्तूबर 2017
Accepted
26 नवम्बर 2017
First published
27 नवम्बर 2017
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2018,9, 22-32

A lesson for site-selective C–H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls

K. Hirano and M. Miura, Chem. Sci., 2018, 9, 22 DOI: 10.1039/C7SC04509C

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