4.8 Article

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

Journal

ACS CATALYSIS
Volume 12, Issue 6, Pages 3279-3285

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c00638

Keywords

photoredox catalysis; sulfur ylides; radical; copper; alkene difunctionalization; multicomponent reactions

Funding

  1. National Natural Science Foundation of China [21971081, 22171099, 21820102003, 91956201]
  2. Open Research Fund of School of Chemistry and Chemical Engineering, Henan Normal University [2021YB02]
  3. Excellent Doctoral Dissertation Cultivation Grant from CCNU
  4. Program of Introducing Talents of Discipline to Universities of China (111 Program) [B17019]

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A visible light-driven photoredox-catalyzed and copper(II)-assisted three-component radical addition/hydroxylation reaction of alkenes, sulfur ylides, and water has been reported, providing high-yielding and practical access to valuable gamma-hydroxy carbonyl compounds.
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.

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