A new preparative method and some chemical properties of 4-R-furazan-3-carboxylic acid amidrazones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2015-04

AUTHORS

Andrei I. Stepanov, Vladimir S. Sannikov, Dmitry V. Dashko, Alexey G. Roslyakov, Alexander A. Astrat’ev, Elena V. Stepanova

ABSTRACT

An alternative method has been developed for the preparation of 4-R-furazan-3-carboxylic acid amidrazones (R = OMe, NH2, substituted amino group) by reductive opening of 1,2,4-oxadiazole ring in 4-R derivatives of (1,2,4-oxadiazol-3-yl)furazans by the action of hydrazine. The starting 1,2,4-oxadiazoles were synthesized from 4-aminofurazan-3-carboxylic acid amidoxime. Some chemical properties of the obtained compounds were studied. More... »

PAGES

350-360

References to SciGraph publications

  • 1988-06. Rearrangements of 5-trifluoromethyl-1,2,4-oxadiazoles by action of ammonia and amines in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1994-04. Ring formation reactions of 4-aminofurazan-3-carboxyamidoximfs in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1990-06. σ-Adducts in the 1,2,4-oxadiazole series in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1965. A review of the chemistry of 1,2,4-oxadiazoles in FORTSCHRITTE DER CHEMISCHEN FORSCHUNG
  • 1984-09. Aminofurazans (review) in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1994-05. Synthesis and properties of 4-amino-3-cyanofurazan in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1989-07. Amidrazones in the synthesis of heterocycles (review) in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2001-05. Reactions of Methyl 4-Aminofurazan-3-carboximidate with Nitrogen-Containing Nucleophiles in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s10593-015-1707-4

    DOI

    http://dx.doi.org/10.1007/s10593-015-1707-4

    DIMENSIONS

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