Synthesis of 1,2,3-Triazolo[1,5-a]Pyridin-8-Ium-3-Olates / Khazhieva I.S., Demkin P.M., Nein J.I., Glukhareva T.V., Morzherin Y.Yu. // Chemistry of Heterocyclic Compounds. - 2015. - V. 51, l. 2. - P. 199-202.

ISSN:

00093122

Type:

Article

Abstract:

[Figure not available: see fulltext.] Alkylation of sodium 4-acetyl-1-phenyl-1,2,3-triazol-5-olate with α-bromoacetophenones was shown to occur at position 3 of the heterocycle, with the formation of 1,2,3-triazol-3-ium-5-olates. Intramolecular crotonic condensation of the latter led to the formation of 1,2,3-triazolo[1,5-a]pyridin-8-ium-3-olates. © 2015 Springer Science+Business Media New York.

Author keywords:

1,2,3-triazol-3-ium-5-olates; 1,2,3-triazoles; alkylation; azoles; crotonic condensation; fused heterocycles; heterocyclization; mesoionic heterocycles; pyridines

Index keywords:

нет данных

DOI:

10.1007/s10593-015-1681-x

Смотреть в Scopus:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-84953362227&doi=10.1007%2fs10593-015-1681-x&partnerID=40&md5=d15fd022a893a1819803582a9f208024

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Link	https://www.scopus.com/inward/record.uri?eid=2-s2.0-84953362227&doi=10.1007%2fs10593-015-1681-x&partnerID=40&md5=d15fd022a893a1819803582a9f208024
Affiliations	Ural Federal University, 19 Mira St., Yekaterinburg, Russian Federation
Author Keywords	1,2,3-triazol-3-ium-5-olates; 1,2,3-triazoles; alkylation; azoles; crotonic condensation; fused heterocycles; heterocyclization; mesoionic heterocycles; pyridines
References	Petronilho, A., Müller-Bunz, H., Albrecht, M., (2012) Chem. Commun., 48, p. 6499. , 1:CAS:528:DC%2BC38XotFyjsLY%3D; Abu-El-Haj, M.J., McFarland, J.W., US Patent 3933843 (1976) Chem. Abstr., 84, p. 121847; Abu-El-Haj, M.J., McFarland, J.W., US Patent 3939174 (1976) Chem. Abstr., 84, p. 164788; Wall, R.J., Bell, D.R., Bazzi, R., Fernandes, A., Rose, M., Rowlands, J.C., Mellor, I.R., (2012) Toxicology, 302, p. 140. , 1:CAS:528:DC%2BC38XhslejtbbP; Wamhoff, H., (1984) Comprehensive Heterocyclic Chemestry, p. 350. , A.R. Katritzky C. Rees (eds) 5 Pergamon Press Oxford; Blume, F., Franke, W., Arndt, F., Rees, R., US Patent 4859230; Abbott, P.A., Bonnert, R.V., Caffrey, M.V., Cage, P.A., Cooke, A.J., Donald, D.K., Furber, M., Withnall, J., (2002) Tetrahedron, 58, p. 3185. , 1:CAS:528:DC%2BD38Xis1Cms7k%3D; Bocian, W., Wiench, J., Stefaniak, L., Webb, G.A., (1996) Magn. Reson. Chem., 34, p. 453. , 1:CAS:528:DyaK28Xjs1yksb8%3D; Nein, Y.I., Pospelova, T.A., Bakulev, V.A., Morzherin, Y.Y., (2005) Chem. Heterocycl. Compd., 41, p. 940. , 1:CAS:528:DC%2BD2MXht1KqsbbF; Nein, Y.I., Gladkova, S.V., Pospelova, T.A., Morzherin, Y.Y., (2006) Chem. Heterocycl. Compd., 42, p. 1472. , 1:CAS:528:DC%2BD2sXjsV2jt7o%3D; Nein, Y.I., Morzherin, Y.Y., Rozin, Y.A., Bakulev, V.A., (2002) Chem. Heterocycl. Compd., 38, p. 1104; Nein, Y.I., Polyakova, A.Y., Morzherin, Y.Y., Savel'Eva, E.A., Rozin, Y.A., Bakulev, V.A., (2004) Russ. J. Org. Chem., 40, p. 879. , 1:CAS:528:DC%2BD2cXotl2jt7g%3D; Nein, Y.I., Morzherin, Y.Y., (2014) Chem. Heterocycl. Compd., 50, p. 1021. , 1:CAS:528:DC%2BC2cXhsFCgsLjL; Savini, L., Massarelli, P., Chiasserini, L., Pellerano, C., Bruni, G., (1994) Farmaco, 49, p. 633. , 1:CAS:528:DyaK2MXitlers7g%3D; Sheldrick, G.M., (2008) Acta Crystallogr., Sect. A: Found. Crystallogr., 64, p. 112
Correspondence Address	Morzherin, Y.Yu.; Ural Federal University, 19 Mira St., Russian Federation; email: yu.yu.morzherin@urfu.ru
Publisher	Springer New York LLC
CODEN	CHCCA
Language of Original Document	English
Abbreviated Source Title	Chem. Heterocycl. Compd.
Source	Scopus