Recent Progress on Reactions of Arylmethyl Azides with Alkenes

被引：1
|
作者：
Li, Xiuying [1 ]
Li, Yajun [2 ]
Wei, Xiansheng [1 ]
Luo, Jinrong [1 ]
Huang, Guobao [1 ]
Tan, Minxiong [1 ]
机构：
[1] Yulin Normal Univ, Guangxi Key Lab Agr Resources Chem & Biotechnol C, Coll Chem & Food Sci, Yulin 537000, Peoples R China
[2] Hunan Polytech Environm & Biol, Coll Med & Technol, Hengyang 421005, Peoples R China
来源：
CHINESE JOURNAL OF ORGANIC CHEMISTRY | 2019年 / 39卷 / 07期
基金：
中国国家自然科学基金;
关键词：
arylmethyl azides; alkenes; reaction mechanism; REGIOSELECTIVE SYNTHESIS; ALKYL AZIDES; 3+2 CYCLOADDITION; CASCADE REACTION; ORGANIC AZIDES; BENZYL AZIDES; 1,2,3-TRIAZOLES; REARRANGEMENT; CHALCONES;
D O I：
10.6023/cjoc201903001
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Arylmethyl azides (ArCH2N3) as one of the significant nitrogen sources with stable properties, simple synthesis, have been widely used in a wide range of organic synthesis reactions. The recent progress (2014 similar to 2018) on reactions of arylmethyl azides with alkenes is summarized. In addition, the organic reactions of arylmethyl azides with types of alkenes are described respectively, with their scope of substrates and reaction mechanism. It is hoped that this review can be referred to the future application in organic synthesis of arylmethyl azides with alkenes.
引用
收藏
页码：1831 / 1836
页数：6
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