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 |
|