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dc.contributor.author | Shtyrlin N. | |
dc.contributor.author | Dobrynin A. | |
dc.contributor.author | Madzhidov T. | |
dc.contributor.author | Pugachev M. | |
dc.contributor.author | Sysoeva L. | |
dc.contributor.author | Musin R. | |
dc.contributor.author | Litvinov I. | |
dc.contributor.author | Klimovitskii E. | |
dc.contributor.author | Shtyrlin Y. | |
dc.date.accessioned | 2018-09-18T20:19:03Z | |
dc.date.available | 2018-09-18T20:19:03Z | |
dc.date.issued | 2011 | |
dc.identifier.issn | 1070-4280 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/138646 | |
dc.description.abstract | © Pleiades Publishing, Ltd., 2011. Synthetic approaches to three cyclic 2,4,5,6-tetrakis(hydroxymethyl)pyridin-3-ol acetonides were developed. Among seven possible mono- and diketals, six-membered cyclic ketal incorporating the hydroxymethyl group in the 4-position turned out to be the most thermodynamically favorable. The experimental data were consistent with the results of quantum-chemical calculations of the Gibbs energies of formation of different acetonides. The structure of the isolated compounds was studied by X-ray diffraction. | |
dc.relation.ispartofseries | Russian Journal of Organic Chemistry | |
dc.title | Experimental and theoretical study on 6-substituted pyridoxine derivatives. Synthesis of Cyclic 2,4,5,6-Tetrakis-(hydroxymethyl)pyridin-3-ol Acetonides | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 1 | |
dc.relation.ispartofseries-volume | 47 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 100 | |
dc.source.id | SCOPUS10704280-2011-47-1-SID84898735821 |