Nickel nanoparticles catalyze cross-coupling reactions in organonickel species, indicating efficient synthetic methods.
Nickel nanoparticle-catalyzed cross-coupling of diazo compounds with O-benzoyl hydroxylamines via a nickel carbene intermediate was disclosed in this work. A nickel nanoparticle catalyst was generated in situ to decompose diazo compounds to afford organonickel species via migratory insertion of nickel carbene intermediates. The silane not only served as a reductant to produce nickel nanoparticles but also provided hydride to facilitate the cross-coupling reaction. This nickel nanoparticle-catalyzed process exhibited distinct reactivities compared with a homogeneous process.
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Tang et al. (2026) studied this question.
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