Organic Letters · 2016 · 69 citations · 66 references
Natural SciencesChemistryCatalysisOrganic ChemistryOrganometallic ChemistryCatalyst DesignCatalytic MechanismsCoordination ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisAllylic FunctionalizationCatalyst Structure - Activity RelationshipsHeterocycle FunctionalizationMild Reaction ConditionsTransition Metal-catalyzed SynthesisTransition-metal-catalyzed FunctionalizationTransition-metal-catalyzed Heterocycle Synthesis
It has been established that the oxidative sp(2) C-H bond allylation with aliphatic alkenes proceeds under mild conditions by using heteroarenes as directing groups and an (electron-deficient η(5)-cyclopentadienyl)rhodium(III) complex, [Cp(E)RhCl2]2, as a precatalyst. In sharp contrast, the use of [Cp*RhCl2]2 instead of [Cp(E)RhCl2]2 led to a complex mixture of products under the same reaction conditions.
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Rhodium Catalyzed Chelation-Assisted C–H Bond Functionalization Reactions
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