Intramolecularly remote functional group migration reactions involving free radicals

被引:2
|
作者
Chen, Fushan [1 ,2 ]
Cao, Zhu [1 ,2 ]
Zhu, Chen [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Zhangjiang Inst Adv Study, Frontiers Sci Ctr Transformat Mol, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Key Lab Mol Engn Chiral Drugs, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
UNACTIVATED C(SP(3))-H BONDS; CYANO MIGRATION; ALKENES; DIFUNCTIONALIZATION; HETEROARYL; REARRANGEMENT;
D O I
10.1039/d4cc05739b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The application of rearrangement reactions offers opportunities for the efficient construction of complex molecules that are challenging to obtain through conventional synthetic methods. However, the development of radical-mediated rearrangements has lagged far behind that of ionic-type rearrangements, due to the uncontrollability of radical species. Along with the recent renaissance in radical chemistry, radical-mediated functional group migration (FGM) reactions provide a versatile platform for the selective incorporation of functional groups across different molecular distances, enabling the construction of intricate molecular architectures. In the past few years, FGM reactions have showcased plentiful reaction modes, rendering precious control in terms of chemo- and regio-selectivities. This feature article summarizes our achievements in radical-mediated FGM reactions, wherein brief discussion of related works from other laboratories is also included. In this feature article, we aim to provide a comprehensive understanding of the progress in this emerging area.
引用
收藏
页码:14912 / 14923
页数:12
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