Citation: Peng Lifen, Peng Chao, Wang Ming, Tang Zilong, Jiao Yinchun, Xu Xinhua. Phosphoryl Protecting Group Enabled Facile Synthesis of Unsymmetrical 1, 3-Diynes by Selective Hay Coupling[J]. Chinese Journal of Organic Chemistry, ;2018, 38(11): 3048-3055. doi: 10.6023/cjoc201805009 shu

Phosphoryl Protecting Group Enabled Facile Synthesis of Unsymmetrical 1, 3-Diynes by Selective Hay Coupling

  • Corresponding author: Peng Lifen, 1060137@hnust.edu.cn Tang Zilong, zltang@hnust.edu.cn
  • Received Date: 2 May 2018
    Revised Date: 30 May 2018
    Available Online: 5 November 2018

    Fund Project: Project supported by the National Natural Science Foundation of China (No. 21402048), the Natural Science Fund Youth Project of Hunan Province (No. 2018JJ3145), the General Project of Hunan Education Department (No. 17C0629) and the Doctoral Foundation of Hunan University of Science and Technology (No. E51693)the General Project of Hunan Education Department 17C0629the Natural Science Fund Youth Project of Hunan Province 2018JJ3145the National Natural Science Foundation of China 21402048the Doctoral Foundation of Hunan University of Science and Technology E51693

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  • A selective Hay coupling reaction of aromatic terminal acetylenes and monophosphoryl-protected diynes was developed. The polarity of Ph2P(O) realized facile isolation of the desired unsymmetrical 1, 3-diynes from by-products. The low reactivity of monophosphoryl-protected diynes reduced the oxidative homocoupling of itself and enhanced the yields of desired products. A number of aromatic terminal acetylenes and monophosphoryl-protected diynes were tolerated in this reaction, and all the corresponding unsymmetrical 1, 3-diynes could be obtained in moderate to good yields. The unsymmetrical 1, 3-diynes could be applied to synthesize unsymmetrical yne-diynes and cyclic polyynes.
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