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Catalytic S_NAr reaction of non-activated fluoroarenes with amines via Ru η~6-arene complexes

机译:Ruη〜6-芳烃配合物催化非活化氟代芳烃与胺的S_NAr催化反应

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摘要

Ru-catalyzed S_NAr reaction of non-activated fluoroarenes with secondary amines proceeded through η~6-arene complexes to give animated products in up to 79% yield.The nucleophilic aromatic substitution (S_NAr) reaction of haloarenes is a widely used transformation in organic syntheses; multi-substituted arenes, including several pharmaceutical products and natural products, have been synthesized using this method. However, the S_NAr reaction generally requires "electron-poor" aromatic compounds with strong electron-withdrawing group(s), such as nitro and cyano groups, because the aromatic ring is intrinsically electron-rich, and haloarenes without electron-withdrawing group(s), namely non-activated haloarenes, are not suitable as electro-philes in the S_NAr reaction.
机译:Ru活化的非活化氟代芳烃与仲胺的S_NAr反应通过η〜6-芳烃配合物进行合成,产率高达79%。卤代芳烃的亲核芳香取代(S_NAr)反应是有机合成中广泛使用的转化反应;使用这种方法已经合成了多取代的芳烃,包括几种药物产品和天然产品。然而,S_NAr反应通常需要具有强吸电子基团的“贫电子”芳族化合物,例如硝基和氰基,因为该芳族环本质上是富电子的,而卤代芳烃没有吸电子基团。 ,即未活化的卤代芳烃,不适合作为S_NAr反应中的亲电子试剂。

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  • 来源
    《Chemical Communications》 |2010年第2期|336-338|共3页
  • 作者单位

    Department of Chemistry and Biochemistry, School of Advanced Science and Engineering, Wasedu University, Shinjuku, Tokyo, 169-8555, Japan;

    Department of Chemistry and Biochemistry, School of Advanced Science and Engineering, Wasedu University, Shinjuku, Tokyo, 169-8555, Japan;

    Department of Chemistry and Biochemistry, School of Advanced Science and Engineering, Wasedu University, Shinjuku, Tokyo, 169-8555, Japan;

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  • 入库时间 2022-08-17 13:23:29

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