研究论文

钯催化下肟醚导向的sp2 C—H键邻位酰氧化反应

  • 蔡海婷 ,
  • 李丹丹 ,
  • 刘姿 ,
  • 王官武
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  • 中国科学技术大学化学系 合肥微尺度物质科学国家实验室 合肥 230026

收稿日期: 2013-02-19

  网络出版日期: 2013-03-21

基金资助

项目受国家自然科学基金(No. 91021004)和安徽省高校省级自然科学研究重大项目(No. KJ2010ZD05)资助.

Palladium-Catalyzed Decarboxylative ortho-Acylation of O-Methyl Ketoximes via Direct sp2 C—H Bond Activation

  • Cai Haiting ,
  • Li Dandan ,
  • Liu Zi ,
  • Wang Guanwu
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  • Department of Chemistry and Hefei National Laboratory for Physical Sciences at Microscale, University of Science and Technology of China, Hefei, Anhui 230026

Received date: 2013-02-19

  Online published: 2013-03-21

Supported by

Project supported by the National Natural Science Foundation of China (No. 91021004) and the Intercollegiate Key Project of Natural Sciences of Anhui Province, China (No. KJ2010ZD05).

摘要

使用醋酸钯作为催化剂, 过硫酸钠和氧化银为氧化剂, 使肟醚导向的底物与苯甲酰甲酸发生sp2 C—H键的邻位酰氧化反应, 从而得到芳香酮类化合物. 该方法对带吸电子基和给电子基的反应物都有很好的适应性, 最高产率可达98%.

本文引用格式

蔡海婷 , 李丹丹 , 刘姿 , 王官武 . 钯催化下肟醚导向的sp2 C—H键邻位酰氧化反应[J]. 化学学报, 2013 , 71(05) : 717 -721 . DOI: 10.6023/A13020198

Abstract

The palladium-catalyzed decarboxylative ortho-acylation of O-methyl ketoximes with α-oxocarboxylic acids in the presence of Na2S2O8 and Ag2O is demonstrated. This protocol can be applied to various O-methyl ketoximes and α-oxocarboxylic acids with both electron-donating and electron-withdrawing groups with products yields up to 98%.

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