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- W4310516638 abstract "The nickel-catalyzed cross-electrophile coupling of 1,2,3-benzotriazin-4(3H)-ones with aryl bromides to generate a diverse array of ortho-arylated benzamide derivatives has been developed. The reaction displayed good functional group tolerance with Zn as the reductant. The key to this transformation is the ring opening of benzotriazinones, which undergo a denitrogenative process to obtain various benzamide derivatives (29 examples, 42-93% yield). The scalability of this transformation was demonstrated." @default.
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- W4310516638 date "2022-12-01" @default.
- W4310516638 modified "2023-10-15" @default.
- W4310516638 title "Nickel-Catalyzed Cross-Electrophile Coupling of 1,2,3-Benzotriazin-4(3<i>H</i>)-ones with Aryl Bromides" @default.
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- W4310516638 doi "https://doi.org/10.1021/acs.joc.2c02246" @default.
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