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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.
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
Linking options:
https://www.mathnet.ru/eng/mendc3116 https://www.mathnet.ru/eng/mendc/v19/i1/p52
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