New transformations of 5-Hydrazino-2-phenyl-1,3-oxazole-4-carbonitrile View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2007-05

AUTHORS

O. V. Shablykin, V. S. Brovarets, B. S. Drach

ABSTRACT

Treatment of 5-hydrazino-2-phenyl-1,3-oxazole-4-carbonitrile with acetylacetone lead to the formation of a substituted pyrazole residue on C5, which enhanced the electrophilicity of the cyano group in position 4 so that it became capable of reacting with hydrogen sulfide, sodium azide, and hydroxylamine. As a result, the corresponding azole fragments were introduced into position 4 of the 5-(1H-pyrazol-1-yl)-1,3-oxazole system. More... »

PAGES

936-939

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363207050210

DOI

http://dx.doi.org/10.1134/s1070363207050210

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1042917003


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