Visible-light organophotoredox-catalyzed fluoroalkyl aminoxylation of unactivated and activated alkenes
An efficient method for the regioselective tetra-, tri-, di- and per-fluoroalkyl aminoxylation of unactivated and activated alkenes has been achieved with various fluorinated alkyl halides and OH-hydroxylamines. This developed photoredox-neutral protocol features versatile transformations to novel tetrafluoroethylene-containing compounds.
Authors
- Jianhua Ji (ORCID: https://orcid.org/0000-0002-3669-4548)
- Kangjie Li (ORCID: https://orcid.org/0000-0001-9287-7392)
- Die Zhang (ORCID: https://orcid.org/0000-0002-1927-8550)
- Xiangzhu Zhou
- Wen Shao (ORCID: https://orcid.org/0000-0002-5427-079X)
- Chun Xu (ORCID: https://orcid.org/0000-0002-3517-8963)
Institutions
- Xiangtan University (CN)
Publication Details
- Journal
- Chemical Communications
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5cc00748h
- Citations
- 2
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 1.58