Chemistry - A European Journal · 2018 · 57 citations · 79 references
Natural SciencesChemistryCatalysisGreen ChemistryInorganic ChemistryRadical ReactionsSulfur ChemistrySulfur CompoundsSulfur DioxideFunctional Group ToleranceReaction Mechanism ElucidationSubstrate ScopeSulfur Dioxide Chemistry
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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The Many Roles for Fluorine in Medicinal Chemistry
William K. Hagmann · Journal of Medicinal Chemistry · 2008 · 3.6K citations · Full text
Practical and innate carbon–hydrogen functionalization of heterocycles
Yuta Fujiwara, Janice A. Dixon, Fionn O’Hara et al. · Nature · 2012 · 924 citations · Full text