Latest Developments on Palladium- and Nickel-Catalyzed Cross-Couplings Using Aryl Chlorides: Suzuki–Miyaura and Buchwald–Hartwig Reactions

Palladium- and nickel-catalyzed cross-couplings are powerful methods for constructing C–C and C–N bonds, particularly through Suzuki–Miyaura and Buchwald–Hartwig reactions. Although aryl iodides, bromides, and triflates are the most commonly used substrates, aryl chlorides are less frequently utilized due to their lower reactivity. However, they are appealing because they are readily available and inexpensive. This short review highlights recent developments on the Suzuki–Miyaura and Buchwald–Hartwig cross-couplings of aryl chlorides, using both homogeneous and heterogeneous catalysis with palladium and nickel. 1 Introduction 2 Suzuki–Miyaura Cross-Couplings 2.1 Homogeneous Palladium Catalysis 2.2 Heterogeneous Palladium Catalysis 2.3 Homogeneous Nickel Catalysis 2.4 Heterogeneous Nickel Catalysis 3 Buchwald–Hartwig Amination Reactions 3.1 Homogeneous Palladium Catalysis 3.2 Heterogeneous Palladium Catalysis 3.3 Homogeneous Nickel Catalysis 3.4 Heterogeneous Nickel Catalysis 4 Conclusion

Object Details

• Location: Deutsche Nationalbibliothek Frankfurt am Main
• Extent: Online-Ressource
• Language: Englisch

References and Relationships

• Bibliographic citation: Latest Developments on Palladium- and Nickel-Catalyzed Cross-Couplings Using Aryl Chlorides: Suzuki–Miyaura and Buchwald–Hartwig Reactions ; day:08 ; month:07 ; year:2024 ; Synthesis ; (08.07.2024)

Contributors, Places and Time

• Contributor: Sen, Abhijit ; Yamada, Yoichi M. A.

Further information

• DOI: 10.1055/a-2344-5677
• URN: urn:nbn:de:101:1-2408221131032.246920734124
• Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
• Last update: 14.08.2025, 10:46 AM CEST