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Mendeleev Communications, 2009, Volume 19, Issue 1, Pages 52–53
DOI: https://doi.org/10.1016/j.mencom.2009.01.021
(Mi mendc3116)
 

This article is cited in 8 scientific papers (total in 8 papers)

Regiodirected synthesis of hydroazolic compounds with the use of thiosemicarbazide

A. A. Anis'kova, A. A. Sazonovb, I. N. Klochkovaa

a Department of Chemistry, N.G. Chernyshevsky Saratov State University, Saratov, Russian Federation
b Research center Nita-Farm, Saratov, Russian Federation
Abstract: Interaction of α,β-unsaturated ketones of furan series with thiosemicarbazide under basic catalysis leads to 3-furyl-2-thiocarbamoylpyrazolines since nitrous nucleophilic centre of a reagent is activated, whereas the products of intermolecular cyclization of thiosemicarbazones under conditions of acid activation of sulfureous nucleophile are spirocyclic furylmethylene-1,3,4-thiadiazolines.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (18.1 Kb)


Citation: A. A. Anis'kov, A. A. Sazonov, I. N. Klochkova, “Regiodirected synthesis of hydroazolic compounds with the use of thiosemicarbazide”, Mendeleev Commun., 19:1 (2009), 52–53
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  • https://www.mathnet.ru/eng/mendc3116
  • https://www.mathnet.ru/eng/mendc/v19/i1/p52
  • This publication is cited in the following 8 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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