An Effective Synthetic Approach to of 2-([5'-Aryl-2,2'-bipyridin]-6-yl)-5-aryl-1,3,4-oxadiazoles

Valieva, M. I.; Starnovskaya, E. S.; Kopchuk, D. S.; Sharafieva, E. R.; Slovesnova, N. V.; Kovalev, I. S.; Nosova, E. V.; Zyryanov, G. V.; Chupakhin, O. N.

doi:10.1134/S1070428023080195

Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/130952

Title:	An Effective Synthetic Approach to of 2-([5'-Aryl-2,2'-bipyridin]-6-yl)-5-aryl-1,3,4-oxadiazoles
Authors:	Valieva, M. I. Starnovskaya, E. S. Kopchuk, D. S. Sharafieva, E. R. Slovesnova, N. V. Kovalev, I. S. Nosova, E. V. Zyryanov, G. V. Chupakhin, O. N.
Issue Date:	2023
Publisher:	Pleiades Publishing
Citation:	Valieva, M, Starnovskaya, E, Kopchuk, D, Sharafieva, E, Slovesnova, N, Kovalev, I, Nosova, E, Zyryanov, G & Chupakhin, O 2023, 'An Effective Synthetic Approach to of 2-([5'-Aryl-2,2'-bipyridin]-6-yl)-5-aryl-1,3,4-oxadiazoles', Russian Journal of Organic Chemistry, Том. 59, № 8, стр. 1445-1448. https://doi.org/10.1134/S1070428023080195 Valieva, M., Starnovskaya, E., Kopchuk, D., Sharafieva, E., Slovesnova, N., Kovalev, I., Nosova, E., Zyryanov, G., & Chupakhin, O. (2023). An Effective Synthetic Approach to of 2-([5'-Aryl-2,2'-bipyridin]-6-yl)-5-aryl-1,3,4-oxadiazoles. Russian Journal of Organic Chemistry, 59(8), 1445-1448. https://doi.org/10.1134/S1070428023080195
Abstract:	Abstract: A convenient synthetic approach to 2-(2,2'-bipyridin-6-yl)-1,3,4-oxadiazole derivatives is proposed, which involves the preparation of 5-aryl-2,2'-bipyridine-6-carboxylic acid esters by the “1,2,4-triazine” methodology and the subsequent construction of the 1,3,4-oxadiazole ring via the modification of the ester group. © 2023, The Author(s).
Keywords:	2-(2,2'-BIPYRIDIN-6-YL)-1,3,4-OXADIAZOLES DEHYDRATION HETEROCYCLIZATION “1,2,4-TRIAZINE” METHODOLOGY
URI:	http://elar.urfu.ru/handle/10995/130952
Access:	info:eu-repo/semantics/openAccess cc-by
License text:	https://creativecommons.org/licenses/by/4.0/
RSCI ID:	64313354
SCOPUS ID:	85176458362
WOS ID:	001104297900016
PURE ID:	48507388
ISSN:	1070-4280
DOI:	10.1134/S1070428023080195
metadata.dc.description.sponsorship:	Russian Science Foundation, RSF: 18-73-10119-P The work was financially supported by the Russian Science Foundation (project no. 18-73-10119-P).
RSCF project card:	18-73-10119
Appears in Collections:	Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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