Visible-Light-Mediated Ring-Opening Geminal Dibromination of Alkenes via Alkoxy Radicals Enabled by Electron Donor–Acceptor Complex
Rong Wei,
Yuan Wang,
Juantao Zhang,
Chunsheng Wu,
Zhenhua Zhang,
Duo Zhang
Affiliations
Rong Wei
State Key Laboratory for Performance and Structure Safety of Petroleum Tubular Goods and Equipment Materials, Tubular Goods Research Institute of CNPC, Xi’an 710077, China
Yuan Wang
State Key Laboratory for Performance and Structure Safety of Petroleum Tubular Goods and Equipment Materials, Tubular Goods Research Institute of CNPC, Xi’an 710077, China
Juantao Zhang
State Key Laboratory for Performance and Structure Safety of Petroleum Tubular Goods and Equipment Materials, Tubular Goods Research Institute of CNPC, Xi’an 710077, China
Chunsheng Wu
National Engineering Laboratory of Low Permeability Oil-Gas Field Exploration and Development, Changqing Oilfield, Xi’an 710018, China
Zhenhua Zhang
State Key Laboratory for Performance and Structure Safety of Petroleum Tubular Goods and Equipment Materials, Tubular Goods Research Institute of CNPC, Xi’an 710077, China
Duo Zhang
Medicine Center, Guangxi University of Science and Technology, Liuzhou 545006, China
An electron donor–acceptor complex was utilized to generate alkoxy radicals from alcohols under mild conditions using visible light. This approach was combined with a hydroxybromination process to achieve the deconstructive functionalization of alkenes, leading to the production of geminal dibromides. Mechanistic investigations indicated the intermediacy of hypervalent iodine (III) compounds.