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dc.contributor.author | Shtyrlin N. | |
dc.contributor.author | Lodochnikova O. | |
dc.contributor.author | Pugachev M. | |
dc.contributor.author | Madzhidov T. | |
dc.contributor.author | Sysoeva L. | |
dc.contributor.author | Litvinov I. | |
dc.contributor.author | Klimovitskii E. | |
dc.contributor.author | Shtyrlin Y. | |
dc.date.accessioned | 2018-09-18T20:19:01Z | |
dc.date.available | 2018-09-18T20:19:01Z | |
dc.date.issued | 2010 | |
dc.identifier.issn | 1070-4280 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/138642 | |
dc.description.abstract | Methods for the preparation of three cyclic 2,3,4-tris(hydroxymethyl)-6- methylpyridin-5-ol acetonides have been developed by variation of the reaction conditions. The six-membered acetonide turned out to be thermodynamically more stable than the seven-membered acetonide and bis-acetonide. The experimental data were consistent with the results of quantum-chemical calculations. The structure of the isolated compounds was proved by X-ray analysis. © 2010 Pleiades Publishing, Ltd. | |
dc.relation.ispartofseries | Russian Journal of Organic Chemistry | |
dc.title | Theoretical and experimental study on cyclic 6-methyl-2,3,4- tris(hydroxymethyl)pyridin-5-ol acetonides | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 4 | |
dc.relation.ispartofseries-volume | 46 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 561 | |
dc.source.id | SCOPUS10704280-2010-46-4-SID77952513922 |