dc.contributor.author |
Klimovitskii A. |
|
dc.contributor.author |
Zvereva E. |
|
dc.contributor.author |
Chmutova G. |
|
dc.contributor.author |
Dobrynin A. |
|
dc.contributor.author |
Fedorenko V. |
|
dc.contributor.author |
Shtyrlin Y. |
|
dc.contributor.author |
Litvinov I. |
|
dc.contributor.author |
Bulygina T. |
|
dc.contributor.author |
Klimovitskii E. |
|
dc.date.accessioned |
2018-09-18T20:05:15Z |
|
dc.date.available |
2018-09-18T20:05:15Z |
|
dc.date.issued |
2007 |
|
dc.identifier.issn |
0022-2860 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/136377 |
|
dc.description.abstract |
IR spectroscopy and ab initio calculations have been applied to the title compounds. Bicyclic acetals were found to exist as mixture of chair and twist-boat conformations, a parent epoxide being in ternary equilibrium. X-ray data on 4-methyl (exo) derivative display a twist-boat form. © 2006 Elsevier B.V. All rights reserved. |
|
dc.relation.ispartofseries |
Journal of Molecular Structure |
|
dc.subject |
ab initio calculations |
|
dc.subject |
IR spectroscopy |
|
dc.subject |
Seven-membered bicyclic acetals |
|
dc.subject |
X-ray crystallography |
|
dc.title |
Conformational isomerism in 3,5,8-trioxabicyclo[5.1.0]octane and its diastereomeric 4-methyl derivatives. A combined IR, X-ray and ab initio study |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
1-3 |
|
dc.relation.ispartofseries-volume |
828 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
147 |
|
dc.source.id |
SCOPUS00222860-2007-828-13-SID33846649158 |
|