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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

Ning Yan, Yi Wang, Ming Bao, Xiaoqiang Yu

2025Angewandte Chemie International Edition8 citationsDOI

Abstract

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.

Topics & Concepts

CatalysisAtom (system on chip)Visible spectrumPhotochemistryChemistryTransfer (computing)PhysicsComputer scienceOrganic chemistryOptoelectronicsOperating systemFluorine in Organic ChemistryRadical Photochemical ReactionsCatalytic C–H Functionalization Methods
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 | Litcius