4.8 Article

Palladium-catalyzed amination of aryl halides on solid support

Journal

ORGANIC LETTERS
Volume 4, Issue 26, Pages 4689-4692

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol027119s

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[GRAPHICS] The first examples of the Pd(0)-catalyzed amination of aryl halides using Rink-resins as nitrogen source are described. Pd(2)dba(3)/BINAP/NaO-t-Bu was found to be the most efficient catalyst/base system, while a solvent mixture of dioxane and tert-butyl alcohol was shown to enhance the selectivity toward the desired monoarylation. Moderate to good yields and excellent purities of the amination products were found with electron-poor aryl halides, while electon-rich aryl halides failed to react under these conditions.

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