研究论文

新颖的银(I)催化磺酰氯与芳香端炔的反应

  • 邓桂胜 ,
  • 孙腾飞 ,
  • 周佳
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  • a 湖南师范大学化学化工学院 长沙 410081;
    b 湖南师范大学化学生物学及中药分析教育部重点实验室 长沙 410081

收稿日期: 2012-04-11

  修回日期: 2012-06-07

  网络出版日期: 2012-06-19

A Novel Silver(I)-Catalyzed Reaction of Terminal Arylacetylenes with Sulfonyl Chlorides

  • Deng Guisheng ,
  • Sun Tengfei ,
  • Zhou Jia
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  • a College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081;
    b Key Laboratory of Chemical Biology & Traditional Chinese Medicine Research (Hunan Normal University), Ministry of Education, Changsha 410081

Received date: 2012-04-11

  Revised date: 2012-06-07

  Online published: 2012-06-19

摘要

报道银(I)催化芳香端炔与磺酰氯的新颖反应. 该反应出乎意料地得到烯基砜, 产率47%~72%, 并且具有Z选择性. 提出了自由基催化循环机理, 解释了烯基砜的形成及烯基砜的立体化学结果.

本文引用格式

邓桂胜 , 孙腾飞 , 周佳 . 新颖的银(I)催化磺酰氯与芳香端炔的反应[J]. 有机化学, 2012 , 32(10) : 1872 -1879 . DOI: 10.6023/cjoc201204011

Abstract

A novel reaction of terminal arylacetylenes with sulfonyl chlorides was performed in the presence of a silver(I) catalyst. Vinyl sulfones were obtained in 47%~72% yields. A free radical mechanism for the catalytic cycle has been proposed to account for the formation of products and the stereochemical outcome of vinyl sulfones.

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