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.
Authors
- Hua‐Jin Xu
- Jie Wang (ORCID: https://orcid.org/0000-0001-8587-1304)
- Hai Liu (ORCID: https://orcid.org/0000-0002-2616-7437)
- Yang Xu (ORCID: https://orcid.org/0009-0005-0245-9020)
- Yaodong Li
- Yi Hu
Institutions
- Nanjing Tech University (CN)
- Bio-oriented Technology Research Advancement Institution (JP)
- State Key Laboratory of Materials-Oriented Chemical Engineering
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