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- W4214717015 endingPage "3285" @default.
- W4214717015 startingPage "3279" @default.
- W4214717015 abstract "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 γ-hydroxy carbonyl compounds. Key to the success of the reaction is the controlled generation of α-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·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 up a platform for further investigation into the radical synthetic chemistry of sulfur ylides." @default.
- W4214717015 created "2022-03-02" @default.
- W4214717015 creator A5016227191 @default.
- W4214717015 creator A5031776909 @default.
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- W4214717015 creator A5080306619 @default.
- W4214717015 creator A5081038018 @default.
- W4214717015 creator A5090345292 @default.
- W4214717015 date "2022-02-25" @default.
- W4214717015 modified "2023-10-16" @default.
- W4214717015 title "Photoredox-Catalyzed and Copper(II) Salt-Assisted Radical Addition/Hydroxylation Reaction of Alkenes, Sulfur Ylides, and Water" @default.
- W4214717015 cites W1595990276 @default.
- W4214717015 cites W1996941025 @default.
- W4214717015 cites W2012373379 @default.
- W4214717015 cites W2012907465 @default.
- W4214717015 cites W2019692171 @default.
- W4214717015 cites W2033620575 @default.
- W4214717015 cites W2040023935 @default.
- W4214717015 cites W2051822378 @default.
- W4214717015 cites W2062233194 @default.
- W4214717015 cites W2064598812 @default.
- W4214717015 cites W2072787851 @default.
- W4214717015 cites W2083334069 @default.
- W4214717015 cites W2090177022 @default.
- W4214717015 cites W2137484199 @default.
- W4214717015 cites W2138868499 @default.
- W4214717015 cites W2159151513 @default.
- W4214717015 cites W2164110244 @default.
- W4214717015 cites W2166214595 @default.
- W4214717015 cites W2215894026 @default.
- W4214717015 cites W2415936852 @default.
- W4214717015 cites W2418726947 @default.
- W4214717015 cites W2466115710 @default.
- W4214717015 cites W2488372015 @default.
- W4214717015 cites W2488628364 @default.
- W4214717015 cites W2520813356 @default.
- W4214717015 cites W2520908811 @default.
- W4214717015 cites W2588298887 @default.
- W4214717015 cites W2626170714 @default.
- W4214717015 cites W2729235130 @default.
- W4214717015 cites W2768059482 @default.
- W4214717015 cites W2779917919 @default.
- W4214717015 cites W2784258588 @default.
- W4214717015 cites W2788670372 @default.
- W4214717015 cites W2797618890 @default.
- W4214717015 cites W2802968297 @default.
- W4214717015 cites W2811084420 @default.
- W4214717015 cites W2871449583 @default.
- W4214717015 cites W2883397411 @default.
- W4214717015 cites W2885154877 @default.
- W4214717015 cites W2892312504 @default.
- W4214717015 cites W2899528819 @default.
- W4214717015 cites W2901709248 @default.
- W4214717015 cites W2906461990 @default.
- W4214717015 cites W2921989892 @default.
- W4214717015 cites W2951527653 @default.
- W4214717015 cites W2952798411 @default.
- W4214717015 cites W2953107731 @default.
- W4214717015 cites W2956147480 @default.
- W4214717015 cites W2966750758 @default.
- W4214717015 cites W2990309671 @default.
- W4214717015 cites W2995044761 @default.
- W4214717015 cites W3008415212 @default.
- W4214717015 cites W3009259094 @default.
- W4214717015 cites W3011414471 @default.
- W4214717015 cites W3015879606 @default.
- W4214717015 cites W3020906212 @default.
- W4214717015 cites W3035107583 @default.
- W4214717015 cites W3042955916 @default.
- W4214717015 cites W3043216838 @default.
- W4214717015 cites W3046931705 @default.
- W4214717015 cites W3083650975 @default.
- W4214717015 cites W3091104178 @default.
- W4214717015 cites W3091522035 @default.
- W4214717015 cites W3104592389 @default.
- W4214717015 cites W3114241796 @default.
- W4214717015 cites W3126387639 @default.
- W4214717015 cites W3156126417 @default.
- W4214717015 cites W3180964617 @default.
- W4214717015 cites W3187051400 @default.
- W4214717015 cites W3194725720 @default.
- W4214717015 cites W3204595699 @default.
- W4214717015 cites W3206658971 @default.
- W4214717015 cites W3211450691 @default.
- W4214717015 cites W3215594211 @default.
- W4214717015 cites W3216830747 @default.
- W4214717015 cites W4200225493 @default.
- W4214717015 cites W4200391456 @default.
- W4214717015 cites W4200407667 @default.
- W4214717015 cites W4205478521 @default.
- W4214717015 cites W4205796187 @default.
- W4214717015 cites W4206591859 @default.
- W4214717015 cites W4207007328 @default.
- W4214717015 cites W4210368278 @default.
- W4214717015 cites W4210568790 @default.
- W4214717015 cites W4361796367 @default.
- W4214717015 doi "https://doi.org/10.1021/acscatal.2c00638" @default.