Organic Letters · 2016 · 49 citations · 44 references
PharmacyChemistryMedicinal ChemistryCatalysisDrug DiscoverySynthetic Medicinal ChemistryDiversity-oriented SynthesisSulfur ChemistryC - C Coupling ReactionsChemical Diversity AnalysisChemoselective Library SynthesisElemental Sulfur ChemistryThiadiazole ChemistryThiazole ChemistryThiazole Synthesis
A copper-mediated, three-component reaction between two different N-Ts hydrazones and elemental sulfur was developed, leading to a series of unsymmetric 2,5-disubstituted 1,3,4-thiadiazoles in moderate yields with good functional group compatibility. This procedure features the employment of elemental sulfur and the selective denitrogenation between aryl and alkyl aldehyde N-tosyl hydrazones, allowing rapid access to unsymmetric 2,5-disubstituted 1,3,4-thiadiazoles frameworks with chemical diversity and complexity.
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U. Salgin-Goksen, Nesrin Gökhan-Kelekçi, O. Goktas et al. · Bioorganic & Medicinal Chemistry · 2007 · 374 citations