Reduction of 7-R derivatives of 7H-tris[1,2,5]oxa-diazolo[3,4-b:3′,4′-d:3″,4″-f]azepine 1-oxide with furoxan ring opening. preparation of 4-R-4H-bis-[1,2,5]oxadiazolo[3,4-b:3′,4′-f]azepine-8,9-diamines View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2013-09-26

AUTHORS

A. I. Stepanov, D. V. Dashko, A. A. Astrat’ev

ABSTRACT

It was shown that the reduction of derivatives of 7-R-7H-tris[1,2,5]oxadiazolo[3,4-b:3′,4′-d:3″,4″-f]azepine 1-oxide by hydrazine hydrate or hydrogen in the presence of palladium on carbon is accompanied by opening of the furoxan ring of the starting compound to the two amino groups and leads to the production of 4-R-4H-bis[1,2,5]oxadiazolo[3,4-b:3′,4′-f]azepine-8,9-diamines. Some chemical properties of the obtained diamino compounds are discussed. More... »

PAGES

1068-1081

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-013-1345-7

DOI

http://dx.doi.org/10.1007/s10593-013-1345-7

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1015923945


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