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DOI: 10.1055/a-1468-1455
C–H Bond Functionalization Using Pd- and Au-Supported Catalysts with Mechanistic Insights of the Active Species
This work was financially supported by a Grant-in-Aid for Scientific Research (B) (Grant no. 19H02755) from the Ministry of Education, Culture, Science, Sports and Technology, Japan, and by the Japan Society for the Promotion of Science (JSPS) and National Natural Science Foundation of China (NSFC) under the Joint Research Program (JRP with NSFC, Grant no. JPJSJRP 20191804).
Abstract
The process of C–H functionalization has been extensively studied as a direct C–C bond-forming reaction with high atomic efficiency. Efforts have also been made on such reactions by using supported catalysts, which are superior in terms of catalyst separation from the reaction mixture and reusability. In this review, an overview of C–H functionalization reactions, especially those involving Pd- and Au-supported catalysts, is presented. In particular, we discuss reaction mechanisms, active species, leaching, reusability, etc.
1 Introduction
2 Types of Supported Metal Catalysts and Their Active Species
3 Modes of C–H Bond Activation
4 Oxidative C–H C–H Coupling of Aryl Compounds
5 C–H C–H Coupling Where One Side Is Aromatic
6 C–H Acylation of Aromatic Compounds and Related Reactions
7 Conclusion
Key words
C–H functionalization - Pd catalysts - Au catalysts - supported nanoparticles - immobilized complexesPublication History
Received: 15 March 2021
Accepted after revision: 26 March 2021
Accepted Manuscript online:
26 March 2021
Article published online:
26 April 2021
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