Issue 16, 2019

Recent developments in decarboxylative cross-coupling reactions between carboxylic acids and N–H compounds

Abstract

Carboxylic acids and their derivatives are ubiquitous compounds in organic chemistry, and are widely commercially available in a large structural variety. Recently, carboxylic acids have been frequently used as non-toxic and environmentally benign alternatives to traditional organohalide coupling partners in various carbon–carbon and carbon–heteroatom cross-coupling reactions. Along this line, several methods have been reported for the synthesis of nitrogen-containing organic compounds through decarboxylative cross-coupling reactions between carboxylic acids and N–H compounds. This review focuses on recent advances and discoveries on these reactions with special attention on the mechanistic aspects of the reactions.

Graphical abstract: Recent developments in decarboxylative cross-coupling reactions between carboxylic acids and N–H compounds

Article information

Article type
Review Article
Submitted
03 фев. 2019
Accepted
04 мар. 2019
First published
18 мар. 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 8964-8976

Recent developments in decarboxylative cross-coupling reactions between carboxylic acids and N–H compounds

S. Arshadi, S. Ebrahimiasl, A. Hosseinian, A. Monfared and E. Vessally, RSC Adv., 2019, 9, 8964 DOI: 10.1039/C9RA00929A

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