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 |
|