Electrochemical Deaminative Carboxylation of Aryltriazenes with CO<sub>2</sub> to Aryl Carboxylic Acids
The utilization of CO<sub>2</sub> as an appealing chemical feedstock for diverse synthetically valuable products is constantly evolving, potentially alleviating chemical production that relies on petrochemistry. Herein we report the first example of the electrochemical deaminative carboxylation of aryltriazenes with CO<sub>2</sub>. The reaction can be performed under mild and catalyst-free conditions by using sustainable methods with CO<sub>2</sub> as a green C<sub>1</sub> building block, efficiently converting a diverse range of readily available aryltriazenes into synthetically valuable carboxylic acids. In particular, the formation of C-C bonds by deaminative carboxylation would be an impactful addition to the synthesis toolbox.
Authors
- Liang‐Nian He (ORCID: https://orcid.org/0000-0002-6067-5937)
- Alexander Olegovich Terent'ev (ORCID: https://orcid.org/0000-0001-8018-031X)
- An‐Guo Wu
- Hongru Li (ORCID: https://orcid.org/0000-0002-4916-2815)
- Lan Zhao (ORCID: https://orcid.org/0000-0003-0316-7001)
Institutions
- Nankai University (CN)
- N.D. Zelinsky Institute of Organic Chemistry (RU)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-04-18
- DOI
- https://doi.org/10.1021/acs.orglett.5c01099
- Citations
- 8
- Primary Topic
- Carbon dioxide utilization in catalysis
- Type
- article
- Field-Weighted Citation Impact
- 5.64
Funders
- National Natural Science Foundation of China
- National Key Research and Development Program of China