The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones

Viktorova, V. V.; Steparuk, E. V.; Obydennov, D. L.; Sosnovskikh, V. Y.

doi:10.3390/molecules28031285

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Полная запись метаданных

Поле DC	Значение	Язык
dc.contributor.author	Viktorova, V. V.	en
dc.contributor.author	Steparuk, E. V.	en
dc.contributor.author	Obydennov, D. L.	en
dc.contributor.author	Sosnovskikh, V. Y.	en
dc.date.accessioned	2024-04-05T16:15:24Z	-
dc.date.available	2024-04-05T16:15:24Z	-
dc.date.issued	2023	-
dc.identifier.citation	Viktorova, VV, Steparuk, EV, Obydennov, DL & Sosnovskikh, VY 2023, 'The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones', Molecules, Том. 28, № 3, 1285. https://doi.org/10.3390/molecules28031285	harvard_pure
dc.identifier.citation	Viktorova, V. V., Steparuk, E. V., Obydennov, D. L., & Sosnovskikh, V. Y. (2023). The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones. Molecules, 28(3), [1285]. https://doi.org/10.3390/molecules28031285	apa_pure
dc.identifier.issn	1420-3049	-
dc.identifier.other	Final	2
dc.identifier.other	All Open Access, Gold, Green	3
dc.identifier.other	https://www.scopus.com/inward/record.uri?eid=2-s2.0-85147893723&doi=10.3390%2fmolecules28031285&partnerID=40&md5=b19e77a9b31090321552940eaca0a5e5	1
dc.identifier.other	https://www.mdpi.com/1420-3049/28/3/1285/pdf?version=1674910466	pdf
dc.identifier.uri	http://elar.urfu.ru/handle/10995/130197	-
dc.description.abstract	This work describes the synthesis of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones, their tautomerism, and reactivity towards binucleophiles. These molecules are novel and convenient building-blocks for the direct construction of biologically important polycyclic pyridones via an oxazinone ring-opening transformation promoted with ammonium acetate or acetic acid. In the case of o-phenylenediamine, partial aromatization of the obtained heterocycles proceeded to form polycyclic benzimidazole-fused pyridones (33–91%). © 2023 by the authors.	en
dc.description.sponsorship	Ministry of Education and Science of the Russian Federation, Minobrnauka	en
dc.description.sponsorship	The research funding from the Ministry of Science and Higher Education of the Russian Federation (Ural Federal University Program of Development within the Priority-2030 Program) is gratefully acknowledged.	en
dc.format.mimetype	application/pdf	en
dc.language.iso	en	en
dc.publisher	MDPI	en
dc.rights	info:eu-repo/semantics/openAccess	en
dc.rights	cc-by	other
dc.rights.uri	https://creativecommons.org/licenses/by/4.0/	unpaywall
dc.source	Molecules	2
dc.source	Molecules	en
dc.subject	4-PYRIDONE	en
dc.subject	ALDEHYDE-LACTOL TAUTOMERISM	en
dc.subject	AMMONIUM ACETATE	en
dc.subject	BENZIMIDAZOLE	en
dc.subject	OXAZINONE	en
dc.subject	RING-OPENING	en
dc.title	The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones	en
dc.type	Article	en
dc.type	info:eu-repo/semantics/article	en
dc.type	\|info:eu-repo/semantics/publishedVersion	en
dc.identifier.doi	10.3390/molecules28031285	-
dc.identifier.scopus	85147893723	-
local.contributor.employee	Viktorova, V.V., Institute of Natural Sciences and Mathematics, Ural Federal University, 51 Lenina Ave, Ekaterinburg, 620000, Russian Federation	en
local.contributor.employee	Steparuk, E.V., Institute of Natural Sciences and Mathematics, Ural Federal University, 51 Lenina Ave, Ekaterinburg, 620000, Russian Federation	en
local.contributor.employee	Obydennov, D.L., Institute of Natural Sciences and Mathematics, Ural Federal University, 51 Lenina Ave, Ekaterinburg, 620000, Russian Federation	en
local.contributor.employee	Sosnovskikh, V.Y., Institute of Natural Sciences and Mathematics, Ural Federal University, 51 Lenina Ave, Ekaterinburg, 620000, Russian Federation	en
local.issue	3	-
local.volume	28	-
dc.identifier.wos	000933749700001	-
local.contributor.department	Institute of Natural Sciences and Mathematics, Ural Federal University, 51 Lenina Ave, Ekaterinburg, 620000, Russian Federation	en
local.identifier.pure	34719285	-
local.description.order	1285	-
local.identifier.eid	2-s2.0-85147893723	-
local.identifier.wos	WOS:000933749700001	-
local.identifier.pmid	36770952	-
Располагается в коллекциях:	Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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