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Palladium-Catalyzed Norbornene-Mediated Tandem <i>ortho</i>-C–H-Amination/<i>ipso</i>-C–I-Cyanation of Iodoarenes: Regiospecific Synthesis of 2-Aminobenzonitrile
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Citations
51
References
2016
Year
Efficient Tandem Ortho-c-h-amination/ipso-cyanationChemical EngineeringMedicinal ChemistryEngineeringCross-coupling ReactionNovel OrganocatalystsRegiospecific SynthesisNatural SciencesOrganic ChemistryOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryAmino FunctionalitiesEnantioselective SynthesisBiomolecular EngineeringPharmaceutical Industry
Efficient tandem ortho-C-H-amination/ipso-cyanation of iodoarenes was accomplished under a norbornene-mediated Pd-catalyzed process. A series of functionalized 2-aminobenzonitriles with much potential in the pharmaceutical industry were obtained by this protocol. This strategy was successfully employed for substitution with two cyano and four amino functionalities in an arene unit in one step under specified conditions.
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