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Simple and Highly Efficient Procedure for Conversion of Aldoximes to Nitriles Using<i>N</i>-(<i>p</i>-Toluenesulfonyl) Imidazole
20
Citations
28
References
2010
Year
Aliphatic OximesDiversity Oriented SynthesisEnantioselective SynthesisEngineeringBiochemistryHighly Efficient ProcedureMedicinePlausible MechanismOrganic ChemistryHeterocycle ChemistryPharmacologyDiverse AldoximesSynthetic ChemistryBiomolecular EngineeringDrug DiscoveryNatural Product Synthesis
A facile and efficient method for dehydration of aldoximes into nitriles using N-(p-toluenesulfonyl) imidazole (TsIm) is described. In this method, aldoximes were refluxed with TsIm in the presence of 1,8-diazabicyclo-[5.4.0]undec-7-ene (DBU) in dimethylformamide (DMF) to afford the corresponding nitriles in good yields. This methodology is highly efficient for various structurally diverse aldoximes including aromatic, heteroaromatic, and aliphatic oximes. A plausible mechanism for the conversion of aldoxime into nitriles using TsIm/DBU is explained.
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