The Journal of Organic Chemistry · 2015 · 55 citations · 36 references
Chemical EngineeringCross-coupling ReactionEngineeringBase-free ProtocolNatural SciencesDiversity-oriented SynthesisOne-pot SynthesisOrganic Chemistry2,5-Diaryl 1,3,4-OxadiazolesCatalysisChemistryHeterocycle ChemistrySynthesis MethodSynthetic ChemistryAryl Tetrazoles
A metal- and base-free protocol for one-pot synthesis of 2,5-diaryl 1,3,4-oxadiazoles via a radical-promoted cross-dehydrogenative coupling strategy was developed. This reaction involved the N-acylation of aryl tetrazoles with aryl aldehydes, followed by thermal rearrangement. A wide range of aryl tetrazoles and aryl aldehydes survived the reaction conditions to deliver the corresponding products in moderate to good yields.
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The electroluminescence of organic materials
Ullrich Mitschke, Peter Bäuerle · Journal of Materials Chemistry · 2000 · 1.7K citations