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
An efficient visible-light-mediated iron-catalyzed atom transfer radical addition (ATRA) reaction between CH<sub>2</sub>Br<sub>2</sub> 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 International Edition
- Published
- 2025-08-19
- DOI
- https://doi.org/10.1002/anie.202511486
- Citations
- 4
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 3.16
Funders
- National Natural Science Foundation of China
- National Key Research and Development Program of China
- Fundamental Research Funds for the Central Universities