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Electrochemical Alkynyl/Alkenyl Migration for the Radical Difunctionalization of Alkenes
61
Citations
83
References
2018
Year
Chemical EngineeringCross-coupling ReactionEngineeringOrganic ElectrochemistryAlkynyl-substituted Tertiary AlcoholsMolecular ElectrochemistryRadical 1,4-Alkynyl MigrationNatural SciencesDiversity-oriented SynthesisElectrosynthesisOrganic ChemistryCatalysisEfficient Electrochemical 1,2-Sulfonylation/alkynylationChemistryRadical DifunctionalizationElectrochemistry
An efficient electrochemical 1,2-sulfonylation/alkynylation of alkenes via radical 1,4-alkynyl migration of alkynyl-substituted tertiary alcohols is described, which used sodium sulfinates as sulfonyl sources affording the corresponding α-sulfonyl-β-alkynylated products in moderate to excellent yields. This electrochemical reaction proceeds smoothly without the use of any metal catalyst, additive and oxidant and thus represents a new and eco-friendly strategy for the difunctionalization of unactive olefins, and also the first example of the electrochemical distal radical migration reaction.
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