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.

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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

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article

Visible‐Light‐Driven Iron‐Catalyzed Atom Transfer Radical Addition of CH2Br2 to Alkenes: Facile Access to 1,3‐Dibromo Compounds

Ming Bao, Ning Yan, Xiaoqiang Yu, Yi Wang
4 citations
Angewandte Chemie International Edition
Fluorine in Organic Chemistry
3.16
article

Visible‐Light‐Driven Iron‐Catalyzed Atom Transfer Radical Addition of CH2Br2 to Alkenes: Facile Access to 1,3‐Dibromo Compounds

Ming Bao, Ning Yan, Xiaoqiang Yu, Yi Wang
article en
4 citations

Abstract

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.

Angewandte Chemie International EditionVol. 64(41)
Dalian University of Technology (CN), Dalian University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 8%
Fluorine in Organic Chemistry
3.16
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