综述与进展

光/电催化下2-芳基-2H-吲唑C-3位的官能团化反应

  • 王丹凤 ,
  • 汪瑾 ,
  • 马春华 ,
  • 姜玉钦 ,
  • 於兵
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  • a 河南师范大学化学化工学院 河南新乡 453007
    b 郑州大学化学学院 郑州 450001

收稿日期: 2022-08-28

  修回日期: 2022-10-13

  网络出版日期: 2022-11-08

基金资助

国家自然科学基金(82003585); 国家自然科学基金(21971224); 河南师范大学优秀科技创新团队(2022TD03); 中国国家级大学生创新创业训练计划(202210476076)

C-3 Functionalization of 2-Aryl-2H-indazoles under Photo/Electrocatalysis

  • Danfeng Wang ,
  • Jin Wang ,
  • Chunhua Ma ,
  • Yuqin Jiang ,
  • Bing Yu
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  • a School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007
    b College of Chemistry, Zhengzhou University, Zhengzhou 450001

Received date: 2022-08-28

  Revised date: 2022-10-13

  Online published: 2022-11-08

Supported by

National Natural Science Foundation of China(82003585); National Natural Science Foundation of China(21971224); Technical Innovation Team of Henan Normal University(2022TD03); National College Students’ Innovation and Entrepreneurship Training Program of China(202210476076)

摘要

2H-吲唑是一种广泛存在于多种上市药物和活性分子中的优势骨架, 对其骨架直接进行C—H键官能团化是构建其衍生物的有效方法之一, 已经成为当前合成化学和药物化学的研究热点. 相比传统的合成方法, 可见光/电化学促进的合成方法条件温和, 是一种环境友好的合成策略. 本文以催化体系分类, 综述了近年来光/电催化下2-芳基-2H-吲唑C-3位的官能团化反应, 特别强调相应的反应机理, 为进一步开发新型的催化方法奠定基础.

本文引用格式

王丹凤 , 汪瑾 , 马春华 , 姜玉钦 , 於兵 . 光/电催化下2-芳基-2H-吲唑C-3位的官能团化反应[J]. 有机化学, 2022 , 42(12) : 4024 -4036 . DOI: 10.6023/cjoc202208039

Abstract

2H-Indazole is a privileged scaffold widely existing in drugs and bioactive molecules. The C—H functionalization of 2H-indazole is the cutting edge in medicinal chemistry and organic chemistry. Compared with traditional synthetic methods, the visible light/electrochemical-promoted synthetic method has mild conditions and is an environmentally friendly synthetic strategy. The C—H functionalization of 2-aryl-2H-indazoles at the C-3 position catalyzed by photochemical/electrochemical strategies in recent years is summarized in terms of catalytic systems, with special emphasis on the corresponding reaction mechanism, which might inspire the further development of new catalytic methods.

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