Heterocyclic Communications · 2017 · 22 citations · 18 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganometallic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisOrganic SynthesisDehydrogenationDehydrogenation ReactionsOxadiazole Chemistry
Abstract A new, simple method for the synthesis of 4 H -1,3,5-oxadiazine derivatives was developed based on the dehydrogenation reaction of N -amidoalkylated thioureas with dicyclohexylcarbodiimide. The reaction was carried out in acetonitrile under reflux for 50–60 min. The precipitated products were easily purified by crystallization from acetonitrile or ethanol. The yields were 30–70%. The structure of the synthesized compounds was determined by IR, 1 H NMR, 13 C NMR, MS and X-ray crystallography.
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A short history of<i>SHELX</i>
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