Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling in Continuous Flow

Carbon–carbon cross-coupling reactions are among the most important processes in organic chemistry and Suzuki–Miyaura reactions are the most widely used protocols. For a decade, green chemistry and particularly catalysis and continuous flow, have shown immense potential in achieving the goals of “gr...

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Bibliographic Details
Main Authors: Christophe Len, Sophie Bruniaux, Frederic Delbecq, Virinder S. Parmar
Format: Article
Language:English
Published: MDPI AG 2017-05-01
Series:Catalysts
Subjects:
Online Access:http://www.mdpi.com/2073-4344/7/5/146
Description
Summary:Carbon–carbon cross-coupling reactions are among the most important processes in organic chemistry and Suzuki–Miyaura reactions are the most widely used protocols. For a decade, green chemistry and particularly catalysis and continuous flow, have shown immense potential in achieving the goals of “greener synthesis”. To date, it seems difficult to conceive the chemistry of the 21st century without the industrialization of continuous flow process in the area of pharmaceuticals, drugs, agrochemicals, polymers, etc. A large variety of palladium Suzuki–Miyaura cross-coupling reactions have been developed using a continuous flow sequence for preparing the desired biaryl derivatives. Our objective is to focus this review on the continuous flow Suzuki–Miyaura cross-coupling using homogeneous and heterogeneous catalysts.
ISSN:2073-4344