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- W2000237248 abstract "Electrochemical reduction of the nitro group in 1-aryl-4-nitroazoles occurs in slightly acidic medium as a typical four-electron process leading to hydroxylamine group formation. The forming 1-aryl-4-hydroxylaminoazoles undergo further reactions. Stability of the hydroxylamines depends on the heteroring (imidazole or pyrazole) and on C-substituents. More stable derivatives condense with the nitroso intermediates to yield azoxycompounds. Less stable hydroxylamines undergo rearrangements, azole ring reduction and decomposition. Some products of these transformations, following the electrochemical reduction, were isolated and their structures were fully characterized by standard methods." @default.
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- W2000237248 date "2000-10-31" @default.
- W2000237248 modified "2023-09-27" @default.
- W2000237248 title "ChemInform Abstract: Electrochemical Reduction of 1-Aryl-4-nitroazoles." @default.
- W2000237248 cites W2949947063 @default.
- W2000237248 doi "https://doi.org/10.1002/chin.200044048" @default.
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