4.8 Article

Transition Metal-Free 1,2-Carboboration of Unactivated Alkenes

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 140, Issue 20, Pages 6221-6225

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b03333

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Funding

  1. WWU Munster
  2. European Research Council (ERC) [692640]

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A method for transition metal-free 1,2-carboboration of unactivated alkenes with bis(catecholato)diboron as the boron source in combination with alkyl halides as the alkyl component is introduced. The three-component reaction proceeds via a radical pathway on a broad range of unactivated alkenes, and the 1,2-carboboration products serve as valuable synthetic building blocks. Density functional theory calculations provide insights into the mechanism.

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