Ontology type: schema:ScholarlyArticle
2013-06
AUTHORSL. V. Batog, V. Yu. Rozhkov, M. I. Struchkova, A. S. Kulikov, N. N. Makhova
ABSTRACT[3+2] Cycloaddition of azide groups of N,N′-bis(4-azidofurazan-3-yl)methylenediamine to 1,3-dicarbonyl compounds and malonodinitrile was shown to proceed regioselectively with the formation of the corresponding N,N′-bis[4-(1H-1,2,3-triazol-1-yl)furazan-3-yl]methylenediamine derivatives. The reactions of N,N′-bis(4-azidofurazan-3-yl)methylenediamine with cyanoacetic acid ethyl ester and amide led to the formation of the product of transformation of the azide group in the starting compound to the amino groups. More... »
PAGES1391-1394
http://scigraph.springernature.com/pub.10.1007/s11172-013-0199-6
DOIhttp://dx.doi.org/10.1007/s11172-013-0199-6
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