Chemistry - A European Journal · 2018 · 75 citations · 30 references
Natural SciencesChemistryOrganic ChemistryOrganometallic ChemistryReaction EngineeringCatalytic MechanismsCross-coupling ReactionsOrganic SynthesisRadical ReactionsReaction MechanismsAlkenyl Halide CouplingOrganolithium AdditionOrganolithium CompoundsRadical Mediated C - H FunctionalizationRadical Reaction MechanismsReaction Coupling
An operationally simple protocol to affect a radical addition to alkenylboronates that spontaneously undergo a [1,2]-metalate shift is described. Overall, the reaction is a three-component coupling of an organolithium, alkenylboronic ester, and halide which takes place with broad scope and good to excellent yields. Experimental mechanistic investigations support the formation of a boron inverse ylid intermediate.
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