| Поле DC | Значение | Язык |
|---|
| dc.contributor.author | Paponov, B. V. | - |
| dc.contributor.author | Rakityansky, D. A. | - |
| dc.contributor.author | Samokhvalova, M. S. | - |
| dc.contributor.author | Denisov, G. L. | - |
| dc.contributor.author | Potapov, A. Yu. | - |
| dc.date.accessioned | 2021-11-23T08:29:50Z | - |
| dc.date.available | 2021-11-23T08:29:50Z | - |
| dc.date.issued | 2021 | - |
| dc.identifier.citation | Ring switching tricomponent synthesis of pyrano[2,3-b]pyridine multifunctional derivatives / B.V. Paponov [et al.] // Mendeleev Communications. - 2021. - №31, №3.-P. 407-408. - Doi: 10.1016/j.mencom.2021.05.041. | ru |
| dc.identifier.uri | http://dspace.bsu.edu.ru/handle/123456789/44303 | - |
| dc.description.abstract | New 3-acylamino-7-hydroxy-5-methyl-2-oxo-2H-pyrano[2,3-b]pyridine-6-carbonitriles were synthesized via a tricomponent condensation of 3-cyano-4-methyl-1,2,5,6-tetrahydropyridine- 2,6-dione, triethyl orthoformate and N-acylglycines under the Erlenmeyer-Plöchl reaction conditions. According to X-ray data, in the solid phase they exist as hydroxypyridine tautomer form | ru |
| dc.language.iso | en | ru |
| dc.subject | chemistry | ru |
| dc.subject | physical chemistry | ru |
| dc.subject | 2H-pyrano[2,3-b]pyridinones | ru |
| dc.subject | 1,2,5,6-tetrahydropyridine-2,6-dione | ru |
| dc.subject | hippuric acid | ru |
| dc.subject | triethyl orthoformate | ru |
| dc.subject | tricomponent condensation | ru |
| dc.subject | ring switching | ru |
| dc.subject | Erlenmeyer-Plöchl reaction | ru |
| dc.title | Ring switching tricomponent synthesis of pyrano[2,3-b]pyridine multifunctional derivatives | ru |
| dc.type | Article | ru |
| Располагается в коллекциях: | Статьи из периодических изданий и сборников (на иностранных языках) = Articles from periodicals and collections (in foreign languages)
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