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Zinc‐Mediated Intermolecular Reductive Radical Fluoroalkylsulfination of Unsaturated Carbon–Carbon Bonds with Fluoroalkyl Bromides and Sulfur Dioxide
57
Citations
79
References
2018
Year
Chemical EngineeringEngineeringUnsaturated Carbon–carbon BondsHeterocyclicFluorous SynthesisFluoroalkyl BromidesOrganic ChemistryOrganometallic CatalysisAvailable Fluoroalkyl BromidesSynthetic ChemistryChemistrySulfur DioxideSulfur Dioxide Anion
A versatile and general zinc-mediated intermolecular reductive radical fluoroalkylsulfination of unsaturated C-C bonds has been developed using readily available fluoroalkyl bromides and 1,4-diazabicyclo[2.2.2]octane-bis(sulfur dioxide) adduct (DABSO) with wide substrate scope and excellent functional group tolerance. Sulfur dioxide anion radical generated in situ from the reduction of sulfur dioxide with zinc may be involved in the reaction mechanism.
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