2022
DOI: 10.1039/d2nj03164g
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Copper catalyzed reaction of alcohols, alkyl halides and Na2S2O3: an odorless and ligand-free route to unsymmetrical thioether synthesis

Abstract: A CuI-catalyzed condensation reaction between alcohols, alkyl halides, and Na2S2O3 leading to structurally diverse thioethers is reported. A variety of alkyl halides and electron-rich benzyl alcohols were employed successfully in...

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Cited by 2 publications
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“…Another key method for the preparation of aryl sulfides is the nucleophilic substitution of sulfides with alcohols, which is mild and efficient, and unsymmetric thioethers can be obtained. 7 In addition, some photocatalytic C–H and C–C functionalization methods are also used in the preparation of thioethers. 8 However, these methods have strict requirements in terms of the steric and electronic properties of substrates, which limits the extension of these strategies.…”
Section: Introductionmentioning
confidence: 99%
“…Another key method for the preparation of aryl sulfides is the nucleophilic substitution of sulfides with alcohols, which is mild and efficient, and unsymmetric thioethers can be obtained. 7 In addition, some photocatalytic C–H and C–C functionalization methods are also used in the preparation of thioethers. 8 However, these methods have strict requirements in terms of the steric and electronic properties of substrates, which limits the extension of these strategies.…”
Section: Introductionmentioning
confidence: 99%