4.8 Article

Arylation of Benzo-Fused 1,4-Quinones by the Addition of Boronic Acids under Dicationic Pd(II)-Catalysis

Journal

ORGANIC LETTERS
Volume 11, Issue 21, Pages 4938-4941

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol902084g

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Funding

  1. UCM-BSCH [GR58/08-910815, CTQ2006-15279-C03-01, SAF2006-04698]

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The first examples of the direct arylation of benzo-fused 1,4-quinones by the dicationic Pd(II)-catalyzed addition of arylboronic acids are reported. The addition reaction is carried out under very mild conditions (dioxane-H2O, rt, open air atmosphere) and is tolerant of free OH groups. In addition, the reaction shows high regioselectivity, when using nonsymmetrical quinones as starting materials.

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