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Nickel-catalyzed aminocarbonylation of Aryl/Alkenyl/Allyl (pseudo)halides with isocyanides and H2O

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Abstract Herein described is a nickel-catalyzed aminocarbonylation of aryl/alkenyl/allyl (pseudo)halides with isocyanides, providing aryl/alkenyl/allyl amides in 41% to 92% yields. Functional groups such as F, Cl, OMe, and heteroaromatic rings… Click to show full abstract

Abstract Herein described is a nickel-catalyzed aminocarbonylation of aryl/alkenyl/allyl (pseudo)halides with isocyanides, providing aryl/alkenyl/allyl amides in 41% to 92% yields. Functional groups such as F, Cl, OMe, and heteroaromatic rings are compatible in the reaction. A Ni(0)/(II) catalytic cycle is proposed based on preliminary experiments and previous literature. The reaction features readily available nickel catalysis, broad functional group tolerance, and simple reaction conditions.

Keywords: aryl alkenyl; alkenyl allyl; nickel catalyzed; catalyzed aminocarbonylation

Journal Title: Tetrahedron Letters
Year Published: 2020

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