Recent advances in 3-aminoindazoles as versatile synthons for the synthesis of nitrogen heterocycles

被引:12
|
作者
Guo, Yimei [1 ]
Gao, Qinghe [1 ]
机构
[1] Xinxiang Med Univ, Sch Pharm, Xinxiang 453003, Henan, Peoples R China
基金
国家重点研发计划;
关键词
OXIDATIVE REARRANGEMENT; ACTIVATED ALKENES; HOFMANN REARRANGEMENT; EFFICIENT; BOND; TRANSANNULATION; CONSTRUCTION; ACCESS; TRANSFORMATIONS; NANOPARTICLES;
D O I
10.1039/d2ob01348g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Nitrogen-based heterocycles are an important class of structural scaffolds distributed in biologically active natural products, medicinal chemistry, and agrochemicals. Hence, there is increasing interest in the development of novel synthetic strategies for the construction of these privileged structural motifs. Recently, 3-aminoindazoles have emerged as versatile synthons participating in a variety of condensation annulation, denitrogenative transannulation and rearrangement ring expansion reactions, which provide efficient synthetic routes for the formation of nitrogen heterocycles. This review systematically highlights for the first time the most recent advances in 3-aminoindazoles to provide a deep understanding of using 3-aminoindazoles as versatile synthons in organic transformations for synthetic and medicinal chemists.
引用
收藏
页码:7138 / 7150
页数:13
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