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Rhenium-Catalyzed Regioselective ortho-Alkenylation and [3+2+1] Cycloaddition of Phenols with Internal Alkynes

机译:铼催化的区域选择性邻烯化酶和[3 + 2 + 1]环加成酚类与内部炔烃

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摘要

An operationally simple and direct rhenium-catalyzed ortho-alkenylation (C-alkenylation) of unprotected phenols with alkynes was developed. The protocol provided ortho-alkenylphenols exclusively, and formation of para- or multiply alkenylated phenols and hydrophenoxylation (O- alkenylation) products were not observed. The [3 + 2 + 1] cycloaddition of phenols and two alkynes via ortho-alkenylation was also demonstrated, in which the alkynes functioned as both two- and one-carbon units. These reactions proceeded with readily available starting materials under neutral conditions without additional ligands.
机译:开发了一种可操作简单且直接的铼催化的邻苯二甲酰化(C-链烯基化)与炔烃的无保护酚。 不观察到提供基于正交 - 链烯基苯酚的邻烯基苯酚和形成脱烯基化酚和疏水氧基化(O-链烯化)产物。 还证明了通过邻烯化化的酚和两种炔烃的循环加入,其中炔烃作为两种和单碳单元起作用。 这些反应在中性条件下易于获得的原料进行,没有其他配体。

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  • 来源
    《Organic letters》 |2019年第9期|共5页
  • 作者单位

    Okayama Univ Grad Sch Nat Sci &

    Technol Div Appl Chem Kita Ku 3-1-1 Tsushimanaka Okayama 7008530 Japan;

    Okayama Univ Grad Sch Nat Sci &

    Technol Div Appl Chem Kita Ku 3-1-1 Tsushimanaka Okayama 7008530 Japan;

    Okayama Univ Grad Sch Nat Sci &

    Technol Div Appl Chem Kita Ku 3-1-1 Tsushimanaka Okayama 7008530 Japan;

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  • 正文语种 eng
  • 中图分类 有机化学;
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