Publication | Closed Access
Nickel-Catalyzed C–CN Bond Formation via Decarbonylative Cyanation of Esters, Amides, and Intramolecular Recombination Fragment Coupling of Acyl Cyanides
80
Citations
63
References
2017
Year
Available EstersChemical EngineeringCross-coupling ReactionEngineeringHeterocyclicNovel OrganocatalystsOrganic Halide CompoundsDecarbonylative CyanationOrganic ChemistryAcyl CyanidesDiazonium SaltsCatalysisOrganometallic CatalysisChemistryHeterocycle ChemistryBiomolecular Engineering
An efficient nickel-catalyzed decarbonylative cyanation reaction which allows the direct functional-group interconversion of readily available esters into the corresponding nitriles was developed. This reaction successfully offers access to structurally diverse nitriles with high efficiency and excellent functional-group tolerance and provides a good alternative to classical synthetic pathways from diazonium salts or organic halide compounds.
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