Nickel-catalyzed reductive coupling of homoenolates and their higher homologues with unactivated alkyl bromides

Homoenolates and their higher homologs have much potential, albeit largely unrealized, in transition metal catalysis. Here, the authors report the nickel-catalyzed generation of homoenolates, and their higher homologs, via decarbonylation of cyclic anhydrides, which then undergo cross-coupling with...

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Autores principales: Tingzhi Lin, Yuanyun Gu, Pengcheng Qian, Haixing Guan, Patrick J. Walsh, Jianyou Mao
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/6bbdb340e93a49b7b63edeb945bf1fc1
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Sumario:Homoenolates and their higher homologs have much potential, albeit largely unrealized, in transition metal catalysis. Here, the authors report the nickel-catalyzed generation of homoenolates, and their higher homologs, via decarbonylation of cyclic anhydrides, which then undergo cross-coupling with alkyl bromides.