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Nickel- vs palladium-catalyzed synthesis of protected phenols from aryl halides

机译:镍和钯催化的芳基卤化物合成保护酚

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摘要

We report the nickel-catalyzed formation of alkyl and silyl ethers from aryl halides in one step. These ethers can act as precursors to phenols by reaction with Bronsted or Lewis acids or with Fluoride, A combination of Ni(COD)_2 and DPPF mediates the formation of tert-butyl aryl, methyl Aryl, and tert-butyldimetryl silyl aryl ethers efficiently from aryl halides and sodium alkloxides or Soldium siloxides under mild reaction conditions.
机译:我们在一个步骤中报告了镍从芳基卤化物催化形成烷基和甲硅烷基醚的镍催化反应。这些醚可通过与布朗斯台德酸或路易斯酸或与氟化物反应而充当酚的前体。Ni(COD)_2和DPPF的组合可有效地形成叔丁基芳基,甲基芳基和叔丁基二甲基甲硅烷基芳基醚在温和的反应条件下,卤化芳基化物和钠的醇盐或Sold的氧化硅。

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