Formation of n-α-diazoacetylureas by the reaction of derivatives of 5-hydroxy-1,2,3-triazole-4-carboxamide with phenylisocyanate and phenyl isothiocyanate / Akat'ev V.E., Bakulev V.A., Mokrushin V.S., Lebedev A.T. // Chemistry of Heterocyclic Compounds. - 1992. - V. 28, l. 10. - P. 1145-1148.

ISSN:

00093122

Type:

Article

Abstract:

The reaction of derivatives of 5-hydroxy-1,2,3-triazole-4-carboxamide with phenyl isocyanate and phenyl isothiocyanate proceeds at the 4-carboxamide fragment of the first, leading to the formation of derivatives of N-phenyl-N′-(2-diazo-2-carbamoylacetyl)urea and -thiourea correspondingly. © 1993 Plenum Publishing Corporation.

Author keywords:

Index keywords:

нет данных

DOI:

10.1007/BF00529576

Смотреть в Scopus:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-34250079472&doi=10.1007%2fBF00529576&partnerID=40&md5=c46dd60c4b33c4afc6b60ff442d14225

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Поле	Значение
Link	https://www.scopus.com/inward/record.uri?eid=2-s2.0-34250079472&doi=10.1007%2fBF00529576&partnerID=40&md5=c46dd60c4b33c4afc6b60ff442d14225
Affiliations	Urals Polytechnic Institute, Ekaterinburg, 620002, Russian Federation
References	Vovk, M.V., Samarai, L.I., (1990) Ukr. Khim. Zh., 12, p. 1313; Franke, K., Ioppien, K., (1986) FRG. Izobret. Stran Mira, 9, p. 56; L'abbe, G., Beenaerts, L., (1989) Bull. Soc. Chim. Belg., 98 (6), p. 419; Nikol, B., (1965) Handbook for the Chemist [in Russian], , B., Nikol'skii, et al., Khimiya, Leningrad; Chimishkyan, A.L., Svetlova, L.P., Monova, T.V., Gulyaev, N.D., (1984) Zh. Obshch. Khim., 7, p. 1477; Dioth, O., (1904) Ann., 335, p. 1; Bchawartz, J., Hornyak, M., Suts, T., (1970) Chem. Ind., 3, p. 92; Shafran, Bakulev, V.A., Mokrushin, V.S., Alekseev, S.G., Lebedev, A.T., Sharbatyan, P.A., (1986) Khim. Geterotsikl. Soedin., 7, p. 926
Correspondence Address	Akat'ev, V.E.; Urals Polytechnic Institute, Ekaterinburg, 620002, Russian Federation
Publisher	Kluwer Academic Publishers-Plenum Publishers
CODEN	CHCCA
Language of Original Document	English
Abbreviated Source Title	Chem Heterocycl Compd
Source	Scopus