DNDMH Enabled C(sp3)−H Nitration of Aryl Alkenes

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2025-01-18 DOI:10.1039/d4cc06671e
Zhiyuan Wang, Yali Li, Xuena Ding, Yuancheng Sun, Chongchong Chen, Wei Sun, Xiangdong Hu
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Abstract

C(sp3)−H bond nitration opens facile access to nitro compounds unreachable from traditional nitration pathway. The work describes herein a C(sp3)−H bond nitration of aryl alkenes with the application of DNDMH, a nitration reagent developed previously in our lab. Notably, this novel nitration process presents good regioselectivity and chemoselectivity between C(sp3)−H nitration and C(sp2)−H nitration.
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DNDMH使C(sp3)−H硝化芳基烯烃
C(sp3)−H键硝化可以方便地获得传统硝化途径无法获得的硝基化合物。本文描述了一种C(sp3)−H键的芳基烯烃硝化与DNDMH的应用,一种硝化试剂,以前在我们的实验室开发。值得注意的是,这种新的硝化过程在C(sp3)−H硝化和C(sp2)−H硝化之间表现出良好的区域选择性和化学选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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