Visible‐Light‐Driven Iron‐Catalyzed Atom Transfer Radical Addition of CH<sub>2</sub>Br<sub>2</sub> to Alkenes: Facile Access to 1,3‐Dibromo Compounds
Abstract An efficient visible‐light‐mediated iron‐catalyzed atom transfer radical addition (ATRA) reaction between CH 2 Br 2 and various alkenes has been developed. This transformation provides direct access to synthetically valuable 1,3‐dibromo compounds with excellent atom economy under mild reaction conditions. The protocol demonstrates remarkable versatility, exhibiting broad substrate scope and excellent functional group compatibility. Notably, the obtained 1,3‐dibromo products function as highly versatile synthetic building blocks. Through rationally designed one‐pot multistep transformations, these intermediates can be conveniently converted into structurally diverse derivatives, including oxetanes and allyl bromides, directly from terminal alkenes.
Authors
- Ming Bao (ORCID: https://orcid.org/0000-0002-5179-3499)
- Ning Yan (ORCID: https://orcid.org/0000-0001-6677-7507)
- Xiaoqiang Yu (ORCID: https://orcid.org/0000-0001-9396-3882)
- Yi Wang (ORCID: https://orcid.org/0000-0002-6541-4584)
Institutions
- Dalian University of Technology (CN)
- Dalian University (CN)
Publication Details
- Journal
- Angewandte Chemie
- Published
- 2025-08-19
- DOI
- https://doi.org/10.1002/ange.202511486
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- National Key Research and Development Program of China
- Fundamental Research Funds for the Central Universities