Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium
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Информация об архиве | Просмотр оригиналаПоле | Значение | |
Заглавие |
Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium
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Автор |
Rammohan, A.
Krinochkin, A. P. Kopchuk, D. S. Shtaitz, Y. K. Sharafieva, E. R. Gaviko, V. S. Zyryanov, G. V. Chupakhin, O. N. |
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Тематика |
2-AMINOOXAZOLES
4,5-DIARYL-3-HYDROXY-2,2′-BIPYRIDINES 5-CYANO-1,2,4-TRIAZINES ANHYDROUS CONDITIONS AZA-DIELS–ALDER REACTION SOLVENT-FREE REACTION |
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Описание |
Abstract: We previously reported the solvent-free reaction of 5-aryl-3-(pyridin-2-yl)-1,2,4-triazine-5-carbo-nitriles with 2-amino-4-aryl-1,3-oxazoles, which afforded 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles. Similar reaction in anhydrous medium led to the formation of two products, previously described 4,5-diaryl-3-hydroxy-2,2′-bipyridine-6-carbonitriles (up to 44%) and 4,5-diaryl-2,2′-bipyridine-6-carbonitriles (up to 32%). © 2023, The Author(s).
Council on grants of the President of the Russian Federation: MK-320.2021.1.3 This study was financially supported by the Council for Grants at the President of the Russian Federation (project no. MK-320.2021.1.3). |
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Дата |
2024-04-05T16:36:43Z
2024-04-05T16:36:43Z 2023 |
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Тип |
Article
Journal article (info:eu-repo/semantics/article) |info:eu-repo/semantics/publishedVersion |
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Идентификатор |
Rammohan, A, Krinochkin, A, Kopchuk, D, Shtaitz, Y, Sharafieva, E, Gaviko, V, Zyryanov, G & Chupakhin, O 2023, 'Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium', Russian Journal of Organic Chemistry, Том. 59, № 9, стр. 1633-1636. https://doi.org/10.1134/S1070428023090233
Rammohan, A., Krinochkin, A., Kopchuk, D., Shtaitz, Y., Sharafieva, E., Gaviko, V., Zyryanov, G., & Chupakhin, O. (2023). Reaction of 3-(Pyridin-2-yl)-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryl-1,3-oxazoles in Anhydrous Medium. Russian Journal of Organic Chemistry, 59(9), 1633-1636. https://doi.org/10.1134/S1070428023090233 1070-4280 Final All Open Access, Hybrid Gold https://www.scopus.com/inward/record.uri?eid=2-s2.0-85177430543&doi=10.1134%2fS1070428023090233&partnerID=40&md5=15595112e9b59f621225a0e406cfbfef https://link.springer.com/content/pdf/10.1134/S1070428023090233.pdf http://elar.urfu.ru/handle/10995/130986 10.1134/S1070428023090233 85177430543 001156603300006 |
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Язык |
en
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Права |
Open access (info:eu-repo/semantics/openAccess)
cc-by https://creativecommons.org/licenses/by/4.0/ |
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Формат |
application/pdf
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Издатель |
Pleiades Publishing
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Источник |
Russian Journal of Organic Chemistry
Russian Journal of Organic Chemistry |
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