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- W2904546809 endingPage "464" @default.
- W2904546809 startingPage "411" @default.
- W2904546809 abstract "Palladium-catalyzed coupling reactions have emerged as powerful tools for the formation of new carbon-carbon bonds. In comparison with other more cost-effective metals such as copper, nickel, and iron, palladium catalysts usually show higher activities and turnover numbers. This makes palladium play an essential role in contemporary chemistry, and has led to its application in the production of pharmaceuticals and fine chemicals. The palladium-catalyzed cross-coupling reaction constitutes one of the most versatile and powerful tools for synthetic organic chemists. Structurally similar, yet diversified, organic molecules can be assembled through a modular approach. This protocol offers a relatively straightforward route for preparing pharmaceutically useful and materially interesting compounds. This chapter summarizes the recent developments of phosphine ligands that enable effective palladium-catalyzed aromatic carbon-nitrogen and carbon-oxygen bond-forming reactions from aryl halides, tosylates, and mesylates. It also describes selected representative examples from mainly 2002-2012." @default.
- W2904546809 created "2018-12-22" @default.
- W2904546809 creator A5005182277 @default.
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- W2904546809 creator A5070751842 @default.
- W2904546809 creator A5083889367 @default.
- W2904546809 creator A5087210340 @default.
- W2904546809 date "2017-11-16" @default.
- W2904546809 modified "2023-09-26" @default.
- W2904546809 title "Cross Coupling Reactions" @default.
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