4.8 Article

Zinc-Catalyzed Dual C-X and C-H Borylation of Aryl Halides

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 54, Issue 40, Pages 11843-11847

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201505603

Keywords

boronate esters; C-H activation; cross-coupling; homogeneous catalysis; nitrogen heterocycles

Funding

  1. DFG
  2. Alexander von Humboldt Foundation

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A zinc-catalyzed combined C-X and C-H borylation of aryl halides using B(2)pin(2) (pin = OCMe2CMe2O) to produce the corresponding 1,2-diborylarenes under mild conditions was developed. Catalytic C-H bond activation occurs ortho to the halide groups if such a site is available or meta to the halide if the ortho position is already substituted. This method thus represents a novel use of a group XII catalyst for C-H borylation. This transformation does not proceed via a free aryne intermediate, but a radical process seems to be involved.

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