Affiliation:
1. Department of Chemical Organic Technology and Petrochemistry,The Silesian University of Technology
Abstract
A series of new 1,3,4-oxadiazoles conjugated to aromatic substituents by an azo linker was synthesized in a four-step reaction sequence, involving cyclodehydration of a N,N'-diacylhydrazine fragment and dehydrogenation of the neighboring hydrazine fragment of the intermediate N,N'-diarylcarbonohydrazide.
Cited by
6 articles.
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1. Synthesis and Characterization of Novel 2-Alkyl-1,3,4-Oxadiazoles Containing a Phenylazo Group;Molecules;2024-09-11
2. Alternative and one-pot synthesis of new conjugated 5-aryl-1,3,4-thiadiazole azo dyes;Dyes and Pigments;2023-12
3. Microwave-Assisted Synthesis of Unsymmetrical 5-Phenyl-1,3,4-oxadiazoles Containing Bis(carboxymethyl)amino Group;Applied Sciences;2023-11-17
4. Synthesis of 2,5-Dialkyl-1,3,4-oxadiazoles Bearing Carboxymethylamino Groups;Molecules;2022-11-09
5. Microwave-promoted synthesis of highly luminescent s-tetrazine-1,3,4-oxadiazole and s-tetrazine-1,3,4-thiadiazole hybrids;Dyes and Pigments;2020-01