The Journal of Organic Chemistry · 2006 · 38 citations · 17 references
Natural SciencesChemistryCatalysisInorganic ChemistryOrganic ChemistryCoordination ChemistryCross-coupling ReactionsHeterocyclic ChemistryMetal-carbon BondingMetal-ligand BondingOrganic SynthesisCarbon-carbon Bond FormationCopper-catalyzed CouplingLigand SelectivityMild Reaction ConditionsTransition Metal-catalyzed SynthesisTransition-metal-catalyzed Functionalization
We present here carbon-nitrogen bond formation via a coupling reaction of 2-iodo-selenophene catalyzed by Cu(I) in the presence of a base and an inexpensive ligand, and establish the first route to obtaining 2-nitrogen-selenophene derivatives in good yields. We can anticipate that this reaction works well with oxazolidinones, lactams, and aliphatic and aromatic amides, as nitrogen sources, in the absence of any supplementary additives. In addition, the reaction proceeded cleanly under mild reaction conditions and was sensitive to the ratio of amide/2-iodo-selenophene, as well as the nature of the ligand, base, and solvent.
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Copper in cross-coupling reactions
I. P. Beletskaya, Andrei V. Cheprakov · Coordination Chemistry Reviews · 2004 · 1.5K citations