Issue 21, 2024, Issue in Progress

Advancements in double decarboxylative coupling reactions of carboxylic acids

Abstract

The double decarboxylative coupling reaction between two (similar or different) molecules of carboxylic acids is an emerging area that has gained considerable attention as a new avenue for forging carbon–carbon bonds. Since this synthetic strategy only utilizes carboxylic acids as easily accessible, non-toxic and stable starting materials, and extrudes carbon dioxide (CO2) as the only waste by-product, it can be considered as an environmentally benign alternative to traditional coupling reactions which mainly rely on the use of toxic organic halides or organometallic reagents. The aim of this review is to highlight the recent advances and developments in this exciting new field that may serve as inspiration for future research to mature it.

Graphical abstract: Advancements in double decarboxylative coupling reactions of carboxylic acids

Article information

Article type
Review Article
Submitted
06 Mar 2024
Accepted
30 Apr 2024
First published
08 May 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 14919-14933

Advancements in double decarboxylative coupling reactions of carboxylic acids

F. Behmagham, M. M. Tawfiq, M. R. Poor Heravi, N. M. A. Alsultany, S. Ballal, H. Bahair, A. H. Adthab, S. Arshadi and E. Vessally, RSC Adv., 2024, 14, 14919 DOI: 10.1039/D4RA01747A

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