Access to Unsymmetric <i>m</i>-Terphenyl Derivatives via Ligand-Promoted Pd-Catalyzed Remote <i>meta</i>-C–H Arylation

Achieving high <i>meta</i>-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 <i>meta</i>-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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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-05-26
DOI
https://doi.org/10.1021/acs.joc.5c00409
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Access to Unsymmetric m-Terphenyl Derivatives via Ligand-Promoted Pd-Catalyzed Remote meta-C–H Arylation

Hua‐Jin Xu, Jie Wang, Hai Liu, Yang Xu et al.
1 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.94
article

Access to Unsymmetric m-Terphenyl Derivatives via Ligand-Promoted Pd-Catalyzed Remote meta-C–H Arylation

Hua‐Jin Xu, Jie Wang, Hai Liu, Yang Xu, Yaodong Li, Yi Hu
article en
1 citations

Abstract

Achieving high <i>meta</i>-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 <i>meta</i>-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.

The Journal of Organic ChemistryVol. 90(22)
Nanjing Tech University (CN), Bio-oriented Technology Research Advancement Institution (JP), State Key Laboratory of Materials-Oriented Chemical Engineering
Openalex Percentile: Top 26%
Catalytic C–H Functionalization Methods
0.94
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