Synlett
DOI: 10.1055/a-2413-0458
synpacts

The Development of Radical/Palladium Relay Catalysis for C–H Carbonylation

Yongzheng Ding
a   Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, 230026, P. R. of China
,
Hanmin Huang
a   Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, 230026, P. R. of China
b   Key Laboratory of Precision and Intelligent Chemistry and Department of Chemistry, University of Science and Technology of China, Hefei, 230026, P. R. of China
› Author Affiliations
We are grateful for financial support from the National Key Research and Development Program of China (2023YFA1507500), the National Natural Science Foundation of China (21925111, 22350008, and 22301289), and the Strategic Priority Research Program of Chinese Academy of Sciences (XDB0450301).


Abstract

The radical/palladium relay catalysis for C–H bond carbonylation is an attractive research topic in synthetic chemistry. It can rapidly prepare carbonylated molecules for synthetic or pharmaceutical applications from highly sought-after feedstocks, such as alkylarenes, alkanes, alkenes, or ethers. The main objective of this Synpacts article is to summarize the development of this research area, mainly focusing on radical/palladium relay catalysis for the carbonylation of single and double C–H bonds.

1 Introduction

2 Radical/Palladium Relay Catalysis for Single C–H Bond Carbonylation Reaction

3 Radical/Palladium Relay Catalysis for Double C–H Bond Carbonylation Reaction

4 Conclusions



Publication History

Received: 04 August 2024

Accepted after revision: 10 September 2024

Accepted Manuscript online:
10 September 2024

Article published online:
08 October 2024

© 2024. Thieme. All rights reserved

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany