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Heterocyclic Scaffolds II: pp 193–234Cite as

Metal-Catalyzed Cross-Coupling Reactions for Indoles

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Part of the book series: Topics in Heterocyclic Chemistry ((TOPICS,volume 26))

Abstract

Metal-catalyzed cross-coupling reactions for indoles are reviewed. Palladium-catalyzed cross-coupling reactions are the most widely explored and applied of all metal-catalyzed cross-coupling reactions. Applications of Kumada coupling, Negishi coupling, Suzuki coupling, Stille coupling, Sonogashira reaction, the Heck reaction, carbonylation, and C–N bond formation reactions in indoles are summarized. In addition, other transition metal-catalyzed cross-coupling reactions using copper, rhodium, iron, and nickel in indole synthesis are also discussed.

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Authors and Affiliations

  1. Discovery Chemistry, Bristol-Myers Squibb Company, 5 Research Parkway, Wallingford, CT, 06492, USA

    Jie Jack Li

  2. Department of Chemistry, 6128 Burke Laboratory, Dartmouth College, Hanover, NH, 03755, USA

    Gordon W. Gribble

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  1. Jie Jack Li
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  2. Gordon W. Gribble
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Correspondence to Jie Jack Li .

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  1. Dept. Chemistry, Dartmouth College, Burke Laboratory 6128, Hanover, 03755, New Hampshire, USA

    Gordon W. Gribble

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Li, J.J., Gribble, G.W. (2010). Metal-Catalyzed Cross-Coupling Reactions for Indoles. In: Gribble, G. (eds) Heterocyclic Scaffolds II:. Topics in Heterocyclic Chemistry, vol 26. Springer, Berlin, Heidelberg. https://doi.org/10.1007/7081_2010_36

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