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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 |