综述与进展

苯炔对双键插入反应的研究进展

  • 吴春蕊 ,
  • 杨玉坡 ,
  • 史峰
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  • a 河南大学 河南省天然药物与免疫工程重点实验室 开封 475004;
    b 青岛科技大学化学与分子工程学院 青岛 266042

收稿日期: 2014-11-26

  修回日期: 2014-12-15

  网络出版日期: 2015-01-09

基金资助

国家自然科学基金(No. 21002021)和河南省高校科技创新人才支持计划基金(No. 13HASTIT010)资助项目.

Recent Advances in Aryne Double Bond Insertion

  • Wu Chunrui ,
  • Yang Yupo ,
  • Shi Feng
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  • a Key Laboratory of Natural Medicine and Immuno-Engineering of Henan Province, Henan University, Kaifeng 475004;
    b College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042

Received date: 2014-11-26

  Revised date: 2014-12-15

  Online published: 2015-01-09

Supported by

Project supported by National Natural Science Foundation of China (No. 21002021) and the Program for Science & Technology Innovation Talents in Universities of Henan Province (No. 13HASTIT010).

摘要

苯炔对双键的插入反应是近年来苯炔化学的一个热点领域. 苯炔对双键插入将产生一个邻亚甲基醌型中间体, 后者和苯炔一样是有机反应的重要活性中间体之一. 综述了近年来苯炔对双键的插入反应及其在合成化学中的应用, 并力图从反应机理的角度对这些插入反应及其生成的中间体进行结构上和反应活性上的阐释.

本文引用格式

吴春蕊 , 杨玉坡 , 史峰 . 苯炔对双键插入反应的研究进展[J]. 有机化学, 2015 , 35(4) : 770 -780 . DOI: 10.6023/cjoc201411041

Abstract

Aryne double bond insertion generates an ortho-quinomethide-typed intermediate, which, like aryne itself, is one of the most important reactive intermediates in organic reactions. This review summarizes recent advances in this field and the potential applications in synthetic organic chemistry, with a focus on the reaction mechanism, as well as the structure and reactivity of the ortho-quinomethide intermediates.

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