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Chloro, Difluoromethylation and Chloro, Carbomethoxydifluoromethylation: Reaction of Radicals Derived from R<sub>f</sub>SO<sub>2</sub>Cl with Unactivated Alkenes under Metal-Free Conditions
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Citations
45
References
2014
Year
Chemical EngineeringMetal-free ConditionsEngineeringRespective Sulfonyl ChloridesAlkene MetathesisCross-coupling ReactionRadical (Chemistry)Fluorous SynthesisOrganic ChemistryCatalysisCarbomethoxydifluoromethyl RadicalsChemistryHalogenationUnactivated Alkenes
Difluoromethyl and carbomethoxydifluoromethyl radicals were generated from their respective sulfonyl chlorides under mild, metal-free conditions leading to efficient atom transfer radical additions (ATRA) to unactivated alkenes to form chloro, difluoromethylated and chloro, carbomethoxydifluoromethylated products.
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