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Copper-catalyzed ortho-acylation of phenols with aryl aldehydes and its application in one-step preparation of xanthones

机译:铜与芳基醛对苯酚的邻位酰化及其在一步法制备氧杂蒽中的应用

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摘要

In the presence of triphenylphosphine, copper(n) chloride can catalyze an intermolecular ortho-acylation reaction of phenols with aryl aldehydes. The reaction proceeds smoothly with a wide range of starting materials, and furthermore, it can be used to synthesize xanthone derivatives in a single step in high yields.
机译:在三苯基膦的存在下,氯化铜可以催化苯酚与芳基醛的分子间邻位酰化反应。该反应在多种起始原料下均能顺利进行,此外,可用于一步一步高产率地合成黄酮衍生物。

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  • 来源
    《Chemical Communications》 |2012年第91期|p.11256-11258|共3页
  • 作者单位

    Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA;

    Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA;

    Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Ministry of Education, Department of Chemistry, Tsinghua University, Beijing 100084, China;

    School of Medicine, University of South Carolina, Columbia, SC 29209, USA;

    Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA;

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  • 入库时间 2022-08-17 13:21:06

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