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Electrochemical reduction of 1-Aryl-4-nitroazoles

Tallec A., Hazard R., Suwiński J., Wagner P.

Polish Journal of Chemistry

2000

Vol. 74, nr 8

1177-1183

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. Some products of this transformations, following the electrochemical reduction, were isolated and their structure were fully characterized by standard methods.