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首页> 外文期刊>Organic letters >Nickel-Catalyzed Denitrogenative Cross-Coupling Reaction of 1,2,3-Benzotriazin-4(3H)-ones with Organoboronic Acids: An Easy Access to Ortho-Arylated and Alkenylated Benzamides
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Nickel-Catalyzed Denitrogenative Cross-Coupling Reaction of 1,2,3-Benzotriazin-4(3H)-ones with Organoboronic Acids: An Easy Access to Ortho-Arylated and Alkenylated Benzamides

机译:镍催化的1,2,3-苯并三嗪-4(3H) - 4-4-4(3H) - 有机硼酸的碳酸盐的交联反应:易于进入邻芳苯胺化和烯基的苯甲酰胺

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摘要

A novel nickel-catalyzed approach to synthesize ortho-arylated and alkenylated benzamides in good to high yields via a denitrogenative cross-coupling reaction of 1,2,3-benzotriazin-4(3H)-ones with organoboronic acids is described. The reaction proceeds through a five-membered azanickelacyclic intermediate with the extrusion of a nitrogen molecule. Moreover, the resulting ortho-arylated benzamides were successfully converted into synthetically useful substituted fluorenones and ortho-arylated benzylamine derivatives in high yields.
机译:描述了一种通过1,2,3-苯并二嗪-4(3H) - 4-4-4-4(3H)酮与有机硼酸的脱氮交联反应合成邻芳苯胺化和链烯化苯胺的新型镍催化方法。 反应通过挤出氮素分子的五元壬虫碱中间体进行。 此外,将得到的邻芳基苯胺成功地转化为合成有用的取代的芴酮和高产率的邻芳基苄胺衍生物。

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