dc.contributor.author |
Soboleva S. |
|
dc.contributor.author |
Gren' A. |
|
dc.contributor.author |
Samitov Y. |
|
dc.contributor.author |
Bogatskii A. |
|
dc.date.accessioned |
2018-09-14T20:06:19Z |
|
dc.date.available |
2018-09-14T20:06:19Z |
|
dc.date.issued |
1972 |
|
dc.identifier.issn |
0009-3122 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/132130 |
|
dc.description.abstract |
The configurations and preferred conformations in series of 4,5-dialkyl and 4,5,5-trialkylsubstituted 2,2-dimethyl-1,3-dioxanes were studied. It was proved by PMR spectroscopy that the low-boiling isomers have the cis configuration, while the high-boiling isomers have the trans configuration; moreover, all of the isomers are found in the preferred chair conformation. This conformation experiences a certain amount of distortion, the degree of which depends on the number and character of the substituents in the 5 position. © 1974 Plenum Publishing Corporation. |
|
dc.relation.ispartofseries |
Chemistry of Heterocyclic Compounds |
|
dc.title |
Stereochemistry of heterocycles - XVII. Configuration and conformation of some stereoisomeric 4,5-substituted 2,2-dimethyl-1,3-dioxanes |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
11 |
|
dc.relation.ispartofseries-volume |
8 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
1321 |
|
dc.source.id |
SCOPUS00093122-1972-8-11-SID34250469915 |
|