Novel synthesis of 3-monosubstituted furoxans

The nitro group in 3-substituted 4-nitrofuroxans (4-nitro-1,2,5-oxadiazol 2-oxides) can be replaced by the hydride ion under the action of NaBH 4 in EtOH, and this reaction is convenient for the preparation of 3-monosubstituted furoxans.

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Bibliographic Details
Published in:Mendeleev communications 1999, Vol.9 (1), p.13-14
Main Authors: Blinnikov, Alexander N., Makhova, Nina N.
Format: Article
Language:English
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Summary:The nitro group in 3-substituted 4-nitrofuroxans (4-nitro-1,2,5-oxadiazol 2-oxides) can be replaced by the hydride ion under the action of NaBH 4 in EtOH, and this reaction is convenient for the preparation of 3-monosubstituted furoxans.
ISSN:0959-9436
DOI:10.1070/MC1999v009n01ABEH000993