Two ways of cyclization of 5-imidazolylthioureas with dimethyl acetylenedicarboxylate / Eltsov O.S., Smirnova M.V., Morzherin Y.Y., Belskaiya N.P., Mokrushin V.S. // Arkivoc. - 2008. - V. 2008, l. 17. - P. 306-317.

ISSN:
1551-7012
Type:
Article
Abstract:
Two ways of cyclization of imidazolyl derivatives of thiourea with dimethylacetylene dicarboxylate (DMAD) were studied. Reaction of N,N'-disubstituted thioureas with DMAD led to formation of a thiazoline ring whereas transformation of trisubstituted thioureas under the same conditions give the novel imidazo[1,5-c][1,3,5]thiadiazine heterocyclic system. © ARKAT USA, Inc.
Author keywords:
DMAD; Heterocyclization; Imidazolylthiourea; Imidazo[1,5-c][1,3,5]thiadiazine; Thiazolidine
Index keywords:
нет данных
DOI:
нет данных
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Affiliations Department of Technology for Organic Synthesis, Urals State Technical University, 19 Mira str., Ekaterinburg 620002, Russian Federation
Author Keywords DMAD; Heterocyclization; Imidazolylthiourea; Imidazo[1,5-c][1,3,5]thiadiazine; Thiazolidine
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Correspondence Address Eltsov, O.S.; Department of Technology for Organic Synthesis, Urals State Technical University, 19 Mira str., Ekaterinburg 620002, Russian Federation; email: oleg-eltsov@yandex.ru
Publisher Arkat
CODEN AGFUA
Language of Original Document English
Abbreviated Source Title Arkivoc
Source Scopus