Synthesis and reactions of thioamides of 5-amino-2-aryl-2H-1,2,3-triazole- 4-carboxylic acid / Belskaya N.P., Sapozhnikova S.G., Bakulev V.A., Eltsov O.S., Slepukhin P.A., Fan Z.-J. // Chemistry of Heterocyclic Compounds. - 2009. - V. 45, l. 7. - P. 844-852.

ISSN:

00093122

Type:

Article

Abstract:

A method has been developed for obtaining thioamides of 5-amino-2-aryl-2H-1,2,3-triazole-4-carboxylic acid. Their heterocyclization reactions with bifunctional reagents has been studied. New heterocyclic polycyclic ensembles have been synthesized containing a 1,2,3-triazole fragment, a thiazole, and a residue of the natural alkaloid cytisine. © 2009 Springer Science+Business Media, Inc.

Author keywords:

α-halo ketones; 1,2,3-triazoles; 1,2,4-triazoles; Aminoimidazoles; Thiazoles; Thioamides; Thioimidinium salts

Index keywords:

нет данных

DOI:

10.1007/s10593-009-0348-x

Смотреть в Scopus:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-70450237178&doi=10.1007%2fs10593-009-0348-x&partnerID=40&md5=d3550d582defcbba8e04a67380a747c6

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Link	https://www.scopus.com/inward/record.uri?eid=2-s2.0-70450237178&doi=10.1007%2fs10593-009-0348-x&partnerID=40&md5=d3550d582defcbba8e04a67380a747c6
Affiliations	Ural State Technological University, Ekaterinburg 620002, Russian Federation; I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, Ekaterinburg 620041, Russian Federation; State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China
Author Keywords	α-halo ketones; 1,2,3-triazoles; 1,2,4-triazoles; Aminoimidazoles; Thiazoles; Thioamides; Thioimidinium salts
References	Belskaya, N.P., Demina, M.A., Sapognikova, S.G., Fan, Z.-J., Zhang H.-Ke, Dehaen, W., Bakulev, V.A., (2008) ARKIVOC, (16), p. 9; Jagodzinski, T.S., (2003) Chem. Rev., 103, p. 197. , 10.1021/cr0200015 1:CAS:528:DC%2BD38XptFOls74%3D; Takahata, H., Yamazaki, T., (1988) Heterocycles, 27, p. 1953. , 10.3987/REV-88-387 1:CAS:528:DyaL1MXpsFSgtA%3D%3D; Abdel-Latif, E., Bondok, S., (2006) Heteroatom. Chem., 17, p. 299. , 10.1002/hc.20206 1:CAS:528:DC%2BD28XkslCgt7s%3D; Hurd, R.N., De Lamater, G., (1961) Chem. Rev., 61, p. 45. , 10.1021/cr60209a003 1:CAS:528:DyaF3MXkt1ymug%3D%3D; Petrov, K.A., Andreev, L.N., (1969) Usp. Khim., 38, p. 41. , 1:CAS:528:DyaF1MXos12jtA%3D%3D; Goddart, C.J.J., (1991) J. Heterocycl. Chem., 28, p. 1607. , 10.1002/jhet.5570280625; Yavari, I., Sayeed-Alangi, S.Z., Hajinasiri, R., Sajjadi-Ghotbabadi, H., (2009) Monatsh. Chem., 140, p. 209. , 10.1007/s00706-008-0065-7 1:CAS:528:DC%2BD1MXpvVaiug%3D%3D; Darehkordi, A., Saidi, K., Islami, M.R., (2007) ARKIVOC, (1), p. 180; Danilkina, N.A., Mikhailov, L.E., Ivin, B.A., (2006) Russ. J. Org. Chem., 42, p. 783. , 10.1134/S1070428006060017 1:CAS:528:DC%2BD28XmvFSgsL8%3D; Acheson, R.M., Wallis, J.D., (1981) J. Chem. Soc., Perkin Trans., 1, p. 415; Solod, O.V., Zelenin, K.N., Pinson, V.V., (1996) Khim. Geterotsikl. Soedin., p. 3. , [Chem. Heterocycl. Comp., 32, 1 (1996)]; Sheldrick, G.M., (1997) SHELXS97. Program for the Solution of Crystal Structures, , Göttingen Univ., Göttingen; Sheldrick, G.M., (1997) SHELXL97. Program for the Refinement of Crystal Structures, , Univ. of Göttingen Göttingen
Correspondence Address	Belskaya, N. P.; Ural State Technological University, Ekaterinburg 620002, Russian Federation; email: belska@mail.ustu.ru
CODEN	CHCCA
Language of Original Document	English
Abbreviated Source Title	Chem. Heterocycl. Compd.
Source	Scopus