Issue 55, 2022
From the journal:

Chemical Communications

New directions in radical carbonylation chemistry: combination with electron catalysis, photocatalysis and ring-opening

Takuji Kawamoto, ORCID logo a   Takahide Fukuyama, ORCID logo b   Baptiste Picard ORCID logo c  and  Ilhyong Ryu ORCID logo *cd  

* Corresponding authors

a Department of Applied Chemistry, Yamaguchi University, Ube, Yamaguchi, Japan

b Department of Chemistry, Osaka Metropolitan University (OMU), Sakai, Osaka, Japan

c Organization for Research Promotion, Osaka Metropolitan University (OMU), Sakai, Osaka, Japan
E-mail: ryu@omu.ac.jp

d Department of Applied Chemistry, National Yang Ming Chiao Tung University (NYCU), Hsinchu, Taiwan

Abstract

Radical carbonylation offers potent methods for introducing carbon monoxide into organic molecules. This feature article focuses on our current efforts to develop new strategies for radical carbonylation, which include electron-transfer carbonylation, site-selective C(sp3)–H carbonylation by a photocatalyst and ring-opening carbonylation.

Graphical abstract: New directions in radical carbonylation chemistry: combination with electron catalysis, photocatalysis and ring-opening

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/D2CC02700C
Article type
Feature Article
Submitted
12 May 2022
Accepted
07 Jun 2022
First published
23 Jun 2022

Chem. Commun., 2022,58, 7608-7617

Permissions

Request permissions

New directions in radical carbonylation chemistry: combination with electron catalysis, photocatalysis and ring-opening

T. Kawamoto, T. Fukuyama, B. Picard and I. Ryu, Chem. Commun., 2022, 58, 7608 DOI: 10.1039/D2CC02700C

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