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Facile C−N Bond Cleavage Promoted by Cuprous Oxide: Formation of C−C-Coupled Biimidazole from Its Methylene-Bridged Congener
42
Citations
38
References
2009
Year
Inorganic ChemistryChemical EngineeringCross-coupling ReactionEngineeringC−c Bond FormationHeterocyclicC−c-coupled BiimidazoleC−n Bond CleavageCovalent Bonded FrameworkCuprous OxideOrganic ChemistryMethylene-bridged CongenerOrganometallic CatalysisChemistryHeterocycle ChemistryBiomolecular Engineering
The methylenebis(N-alkylimidazolium) halides are converted to dialkylbiimidazoles by cuprous oxide with concurrent C−N bond cleavage and C−C bond formation. This unusual C−N bond cleavage is proposed to involve a Cu(I)−NHC (N-heterocyclic carbene) complex. The reaction is unique, as it involves C−H bond activation, C−N bond cleavage, and C−C bond formation.
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