A dual-radical process for tri/di-fluoromethylarylation of alkenes enabled by indirect electroreduction
This study presents a stable and mild electrochemical dual-radical strategy for tri/di-fluoromethylarylation of alkenes. The synergistic combination of cyanoarene and phenanthrene as dual redox mediators constructs an efficient catalytic system.
Authors
- Yuanyuan Xie (ORCID: https://orcid.org/0000-0001-8482-9948)
- Changjun Zhang (ORCID: https://orcid.org/0000-0002-7088-146X)
- Yuxin Ding
- Yuanzhi Shi (ORCID: https://orcid.org/0000-0002-7234-0341)
- Zhening Jin
- Z. P. Zheng
- Wei Ke Su
Institutions
- Ministry of Education (NZ)
- Zhejiang University of Technology (CN)
Publication Details
- Journal
- Chemical Communications
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5cc00744e
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00