REVIEW

Recent Advances in the Coupling Reactions of Arylhydrazine via C—N Bond Cleavage

  • Liu Jinbiao ,
  • Yuan Sitian ,
  • Song Xixi ,
  • Qiu Guanyinsheng
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  • a School of Metallurgy and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000;
    b College of Biological, Chemical Science and Engineering, Jiaxing University, Jiaxing 314001

Received date: 2016-01-28

  Revised date: 2016-04-15

  Online published: 2016-05-03

Supported by

Project supported by the National Natural Science Foundation of China (Nos. 21502075, 21502069, 201502069), the National Natural Science Foundation of Zhejiang Province (No. LQ15B020006) and the Foundation from Zhejiang Education Department (No. Y201431173).

Abstract

As a special synthons containing C—N bond, hydrazine chemistry has attracted a growing interest of chemists due to its versatility in cross-coupling arylation. This review summarizes the recent advances in the coupling reactions of arylhydrazine, which is utilized as an effective arylation reagent in radical reactions, and transition metal-catalyzed homocoupling, Suzuki coupling and Heck coupling via C—N bond cleavage.

Cite this article

Liu Jinbiao , Yuan Sitian , Song Xixi , Qiu Guanyinsheng . Recent Advances in the Coupling Reactions of Arylhydrazine via C—N Bond Cleavage[J]. Chinese Journal of Organic Chemistry, 2016 , 36(8) : 1790 -1796 . DOI: 10.6023/cjoc201601037

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