通过配体促进的pd催化远端间羟基芳基化获得不对称间terphenyl衍生物。

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Xu Yang,Hai Liu,Yao-Dong Li,Jie Wang,Hua-Jin Xu,Yi Hu
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引用次数: 0

摘要

实现低电子苯甲酸衍生物的高间选择性C-H基化仍然是一个艰巨的挑战,这可能是构建不对称1,3-二取代苯衍生物的有效方案。本文报道了配体促进的苯甲酸衍生物的高选择性C-H基化反应。得到了各种不对称和非官能化的1,3-二取代苯衍生物。该策略不仅为各种不对称的1,3-二取代苯衍生物提供了一种简便、模块化和稳健的方法,而且还展示了其他电子贫底物的远程碳氢功能化的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Access to Unsymmetric m-Terphenyl Derivatives via Ligand-Promoted Pd-Catalyzed Remote meta-C-H Arylation.
Achieving high meta-selective C-H arylation of electron-poor benzoic acid derivatives is still a daunting challenge, which could be an efficient protocol to construct unsymmetrical 1,3-disubstituted benzene derivatives. Herein, we report the ligand-promoted high meta-selective C-H arylation of benzoic acid derivatives. A wide range of unsymmetric and unfunctionalized 1,3-disubstituted benzene derivatives were obtained. This strategy not only provided a facile, modular, and robust approach to various unsymmetrical 1,3-disubstituted benzene derivatives but also demonstrated the potential of remote C-H functionalization of other electron-poor substrates.
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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