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Reaction of 5-hydrazono-1,2,3-thiadiazoles with toluene and xylene in the presence of PCl5 Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 2003, Volume: 39, Number: 1, Pages: 126-127 Pages count : 2 DOI: 10.1023/A:1023041329732
Tags 1,2,3-thiadiazole; 1,2,3-triazole; Dimroth rearrangement
Authors Glukhareva T.V. 1 , Dyudya L.V. 1 , Morzherin Yu.Yu. 1 , Tkachev A.V. 2 , Bakulev V.A. 1
Affiliations
1 (Scopus) Urals State Technical University, Yekaterinburg 620002, Russian Federation
2 (Scopus) Novosibirsk Inst. of Organ. Chem., Novosibirsk 630090, Russian Federation

Abstract: The treatment of 5-hydrazono-1,2,3-thiadiazoles by phosphorus pentachloride in toluene or xylene leads to an anomalous Dimroth rearrangement and the reaction of the mercapto function formed with the methyl group of the solvent to give 5-benzylmercapto-1,2,3-triazole.
Cite: Glukhareva T.V. , Dyudya L.V. , Morzherin Y.Y. , Tkachev A.V. , Bakulev V.A.
Reaction of 5-hydrazono-1,2,3-thiadiazoles with toluene and xylene in the presence of PCl5
Chemistry of Heterocyclic Compounds. 2003. V.39. N1. P.126-127. DOI: 10.1023/A:1023041329732 Scopus РИНЦ OpenAlex
Identifiers:
Scopus: 2-s2.0-0037567345
Elibrary: 13438297
OpenAlex: W2950927134
Citing:
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Scopus 3
Elibrary 4
OpenAlex 4
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