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Methylenecyclopropane Annulation by Manganese(I)‐Catalyzed Stereoselective C−H/C−C Activation
41
Citations
77
References
2017
Year
Chemical EngineeringEngineeringNatural SciencesDiversity-oriented SynthesisAbstract C−h/c−c FunctionalizationsVersatile Base‐metal CatalystCatalytic SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisMolecular CatalysisChemistryMethylenecyclopropane AnnulationRobust Manganese
Abstract C−H/C−C functionalizations with methylenecyclopropanes (MCPs) were accomplished with a versatile base‐metal catalyst. A robust manganese(I) complex enabled the expedient annulation of MCPs by synthetically meaningful ketimines to deliver, upon one‐pot hydroarylation, densely substituted polycylic anilines in a step‐economical fashion. Mechanistic studies provided strong support for a facile organometallic C−H manganation, while typical cobalt, ruthenium, rhodium, and palladium catalysts were found completely ineffective.
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