4.8 Article

Selective hydroboration of unsaturated bonds by an easily accessible heterotopic cobalt catalyst

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NATURE COMMUNICATIONS
卷 12, 期 1, 页码 -

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NATURE RESEARCH
DOI: 10.1038/s41467-021-24117-5

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  1. National Natural Science Foundation of China [21821002]
  2. Shanghai Pujiang Program [19PJ1411500]

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A catalytic system utilizing a mixture of cobalt (II) iodide and potassium tert-butoxide has been discovered to be highly active for the hydroboration of vinylarenes and organic nitriles, producing diverse products with high yield and facilitating one-pot transformations. The activation strategy of alkoxide-pinacolborane combination effectively activates cobalt (II) iodide to generate catalytically active heterotopic cobalt catalysts in situ.
Homogeneous earth-abundant metal catalysis based on well-defined molecular complexes has achieved great advance in synthetic methodologies. However, sophisticated ligand, hazardous activator and multistep synthesis starting from base metal salts are generally required for the generation of active molecular catalysts, which may hinder their broad application in large scale organic synthesis. Therefore, the development of metal cluster catalysts formed in situ from simple earth-abundant metal salts is of importance for the practical utilization of base metal resource, yet it is still in its infancy. Herein, a mixture of catalytic amounts of cobalt (II) iodide and potassium tert-butoxide is discovered to be highly active for selective hydroboration of vinylarenes and dihydroboration of nitriles, affording a good yield of diversified hydroboration products that without isolation can readily undergo further one pot transformations. It should be highlighted that the alkoxide-pinacolborane combination acts as an efficient activation strategy to activate cobalt (II) iodide for the generation of metastable heterotopic cobalt catalysts in situ, which is proposed to be catalytically active species. Homogeneous earth-abundant metal catalysis based on well-defined metal complexes is of interest for organic synthesis, but typically employs expensive catalysts, air sensitive or synthetically challenging chemicals. Here, the authors report an efficient and regio-selective catalytic system for hydroboration of vinylarenes and organic nitriles with HBPin, using commercially available CoI2 and (KOBu)-Bu-t under ligand-free conditions.

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