Photoredox-Catalyzed and Copper(II) Salt-Assisted Radical Addition/Hydroxylation Reaction of Alkenes, Sulfur Ylides, and Water

被引:51
作者
Yan, Dong-Mei [1 ]
Xu, Shuang-Hua [1 ]
Qan, Hao [1 ]
Gao, Pan-Pan [1 ]
Bi, Ming-Hang [1 ]
Xiao, Wen-Jing [1 ]
Chen, Jia-Rong [1 ,2 ]
机构
[1] Cent China Normal Univ, CCNU uOttawa Joint Res Ctr, Key Lab Pesticides & Chem Biol, Minist Educ,Coll Chem, Wuhan 430079, Hubei, Peoples R China
[2] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
photoredox catalysis; sulfur ylides; radical; copper; alkene difunctionalization; multicomponent reactions; COUPLED ELECTRON-TRANSFER; C-H FUNCTIONALIZATION; CYCLIZATION REACTIONS; SULFONIUM SALTS; BOND-CLEAVAGE; LIGHT; EPOXIDATION; REDUCTIONS; ALKYLATION; PHOTOLYSIS;
D O I
10.1021/acscatal.2c00638
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A visible light-driven photoredox-catalyzed and copper(II)-assisted three-component radical addition/hydroxylation reaction of alkenes, sulfur ylides, and water is reported. This process shows broad substrate scope and high functional group tolerance, with respect to both readily available sulfur ylides and alkenes, providing high-yielding and practical access to valuable gamma-hydroxy carbonyl compounds. Key to the success of the reaction is the controlled generation of alpha-carbonyl carbon radicals from sulfur ylides via sulfonium salts by a visible-light-driven proton-coupled electron transfer (PCET) strategy in a mixture of 2,2,2-trifluoroethanol/CH2Cl2. Addition of Cu(TFA)(2)center dot H2O helps to accelerate the radical-cation crossover to improve the reaction efficiency. Mechanistic studies suggest that the hydroxy moiety in the products stems from water. This study also builds platform for further investigation into the radical synthetic chemistry of sulfur ylides.
引用
收藏
页码:3279 / 3285
页数:7
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