Publication | Closed Access
New one step synthesis of 3,5‐disubstituted 1,2,4‐oxadiazoles
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Citations
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References
2007
Year
Combinatorial ChemistryChemical EngineeringEthylene GlycolMass SpectroscopyEngineeringNatural SciencesC NmrDiversity-oriented SynthesisOrganic ChemistryChemistryHeterocycle ChemistryNew OneSynthesis Method
Abstract magnified image Disubstituted 1,2,4‐oxadiazoles have been synthesized in good yields and good purity in one pot procedure by reaction of aromatic nitriles, hydroxylamine hydrochloride and sodium carbonate in ethylene glycol under heating at 195°C. The structures of different 1,2,4‐oxadiazoles obtained were confirmed by 1 H, 13 C NMR and mass spectroscopy.
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