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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Highly Efficient Construction of Benzene Ring in Carbazoles by Palladium-Catalyzed endo-Mode Oxidative Cyclization of 3-(3'-Alkenyl)indoles.

A highly efficient construction of the benzene ring in carbazoles by palladium-catalyzed endo-mode oxidative cyclization of 3-(3'-alkenyl)indoles was developed. The reaction utilizes benzoquinone as the stoichiometric oxidant and is conducted under mild conditions.[1]

References

  1. Highly Efficient Construction of Benzene Ring in Carbazoles by Palladium-Catalyzed endo-Mode Oxidative Cyclization of 3-(3'-Alkenyl)indoles. Kong, A., Han, X., Lu, X. Org. Lett. (2006) [Pubmed]
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