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Palladium-catalyzed decarboxylative cross-coupling reaction of cinnamic acid with aryl iodide

机译:肉桂酸与碘代芳基钯的钯催化脱羧交叉偶联反应

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摘要

A highly effective decarboxylative cross-coupling reaction of cinnamic acid with aryl iodide catalyzed by the combination of palladium chloride and CyJohnPhos in the presence of Ag_2CO_3 as an additive is described. The desired carbon-carbon bond formation proceeds efficiently with good functional-group tolerance.rnRecently, the decarboxylative cross-coupling reaction has attracted much attention since it opens a new avenue for carbon-carbon formation. As highlighted by Baudoin, this method has several advantages over the conventional transition metal-catalyzed cross-coupling reactions and the direct arylation through C-H activation, concerning the regioselectivity as well as atom and step economy issues.
机译:描述了在Ag_2CO_3作为添加剂存在下,通过氯化钯和CyJohnPhos的组合催化的肉桂酸与芳基碘的高效脱羧交叉偶联反应。期望的碳-碳键的形成以良好的官能团耐受性有效地进行。最近,脱羧交叉偶联反应由于为碳-碳形成开辟了新途径而引起了广泛的关注。正如Baudoin所强调的,该方法相对于传统的过渡金属催化的交叉偶联反应和通过C-H活化的直接芳基化具有几个优势,涉及区域选择性以及原子和步骤经济性问题。

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  • 来源
    《Organic & biomolecular chemistry》 |2009年第1期|863-865|共3页
  • 作者单位

    Department of Chemistry, Fudan University, 220 Handan Road, Shanghai, 200433, China;

    Department of Chemistry, Fudan University, 220 Handan Road, Shanghai, 200433, China;

    Department of Chemistry, Fudan University, 220 Handan Road, Shanghai, 200433, China;

    Department of Chemistry, Fudan University, 220 Handan Road, Shanghai, 200433, China State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai, 200032, China;

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