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Nickel-Catalyzed Formation of Cyclopentenone Derivatives via the Unique Cycloaddition of α,β-Unsaturated Phenyl Esters with Alkynes

机译:通过α,β-不饱和苯基酯与炔烃的独特环加成反应,镍催化形成环戊烯酮衍生物

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摘要

Oxygen-containing organic compounds, such as ethers, carboxylates, and carbamates, have recently received increasing attention because of their newly discovered applications as electrophiles in cross-coupling reactions via transition metal-catalyzed C-O bond activation. However, no cycloaddition reaction involving their C-O bond activation has been demonstrated thus far. The present study developed a Ni(0)-catalyzed unique [3+2] cycloaddition reaction of α,β-unsaturated phenyl esters with alkynes in 'PrOH to yield cyclopentenone derivatives.
机译:含氧有机化合物,例如醚,羧酸盐和氨基甲酸酯,由于在过渡金属催化的C-O键活化的交叉偶联反应中作为亲电试剂的新发现,最近受到越来越多的关注。然而,到目前为止,尚未证明涉及其C-O键活化的环加成反应。本研究开发了Ni(0)催化的α,β-不饱和苯基酯与炔在'PrOH'中的独特[3 + 2]环加成反应,生成环戊烯酮衍生物。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第38期|p.14900-14903|共4页
  • 作者单位

    Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan,Center for Atomic and Molecular Technologies, Osaka University, Suita, Osaka 565-0871, Japan;

    Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan;

    Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:14:27

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