Abstract
The 1,3,4-oxadiazole is a widely encountered motif in the areas of pharmaceuticals, materials, and agrochemicals. This work has established a mediated electrochemical synthesis of 2,5-disubstituted 1,3,4-oxadiazoles from N-acyl hydrazones. Using DABCO as the optimal redox mediator has enabled a mild oxidative cyclisation, without recourse to stoichiometric oxidants. In contrast to previous methods, this indirect electrochemical oxidation has enabled a broad range of substrates to be accessed, with yields of up to 83 %, and on gram scale. The simplicity of the method has been further demonstrated by the development of a one-pot procedure, directly transforming readily available aldehydes and hydrazides into valuable heterocycles.
Original language | English |
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Number of pages | 10 |
Journal | Chemistry - A European Journal |
Early online date | 18 Sept 2024 |
DOIs | |
Publication status | E-pub ahead of print - 18 Sept 2024 |
Keywords
- 1,3,4-oxadiazoles
- electrochemistry
- hydrazones
- indirect electrolysis
- oxidation