3-Amino-4-[5-(chloromethyl)-1,2,4-oxadiazol-3-yl]furazan –a multifunctional synthon for the synthesis of 1,2,5-oxadiazole derivatives View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-12-28

AUTHORS

Andrei I. Stepanov, Dmitry V. Dashko, Elena V. Stepanova

ABSTRACT

The chemical properties of 3-amino-4-[5-(chloromethyl)-1,2,4-oxadiazol-3-yl]furazan were scrutinized: acylation of the amino group and its oxidation to azo and nitro groups, reactions of the chloromethyl group with N- and S-nucleophilic reagents, as well as reactions of transformation of the 1,2,4-oxadiazole ring.

PAGES

1233-1244

References to SciGraph publications

  • 2015-04. A new preparative method and some chemical properties of 4-R-furazan-3-carboxylic acid amidrazones in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2017-06. 3-Alkyl-4-nitrofurazans – plasticizers for polymers in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1984-09. Aminofurazans (review) in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2017-06. Synthesis and characterization of multicyclic oxadiazoles and 1-hydroxytetrazoles as energetic materials in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2017-09. Rearrangements of 1,2,4-Oxadiazole: “One Ring to Rule Them All” in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1994-01. A convenient synthesis of 3-substituted 5-guanidino-1,2,4-oxadiazoles in RUSSIAN CHEMICAL BULLETIN
  • 2017-06. A rational method of synthesis and chemical properties of 5-(4-aminofurazan-3-yl)-1-hydroxytetrazole in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2013-02. NMR spectroscopic study of 3-nitrofurazans in RUSSIAN CHEMICAL BULLETIN
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    http://scigraph.springernature.com/pub.10.1007/s10593-019-02607-1

    DOI

    http://dx.doi.org/10.1007/s10593-019-02607-1

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