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Chinese Journal of Organic Chemistry >

2017 , Vol. 37 >Issue 4: 824 - 840

DOI: https://doi.org/10.6023/cjoc201611017

REVIEW

Recent Advances in 3-Isothiocyanato Oxindoles Engaged Asymmetric Cascade Reactions

  • Tan Fen ,
  • Xiao Wenjing ,
  • Zeng Guoping
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  • a. Hubei Key Laboratory of Purification and Application of Plant Anti-cancer Active Ingredients, Hubei University of Education, Wuhan 430205;
    b. Key Laboratory of Pesticide & Chemical Biology Ministry of Education and College of Chemistry, Central China Normal University, Wuhan 430079

Received date: 2016-11-15

  Revised date: 2016-12-21

  Online published: 2017-01-04

Supported by

Project supported by the National Natural Science Foundation of China (No. 21602052) and the Scientific Research Project of Hubei Provincial Department of Education (No. Q20163004).

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Abstract

3-Isothiocyanato oxindoles have been widely employed as a class of highly reactive and novel reagents in the enantioselective synthesis of diverse spirooxindoles. This review summarizes the recent advances of 3-isothiocyanato oxindoles mediated some types of cascade process in the past six years, including properties of reaction, activation models and synthetic applications. Furthermore, the prospects of this concept are also discussed.

Key words： 3-isothiocyanato oxindole; spirooxindole; asymmetric synthesis; cascade reaction

Cite this article

Tan Fen , Xiao Wenjing , Zeng Guoping . Recent Advances in 3-Isothiocyanato Oxindoles Engaged Asymmetric Cascade Reactions[J]. Chinese Journal of Organic Chemistry, 2017 , 37(4) : 824 -840 . DOI: 10.6023/cjoc201611017

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