dc.contributor.author |
Samitov Y. |
|
dc.contributor.author |
Zelikman Z. |
|
dc.contributor.author |
Shkrebets A. |
|
dc.contributor.author |
Kul'nevich V. |
|
dc.date.accessioned |
2018-09-14T20:06:30Z |
|
dc.date.available |
2018-09-14T20:06:30Z |
|
dc.date.issued |
1974 |
|
dc.identifier.issn |
0009-3122 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/132134 |
|
dc.description.abstract |
The configuration and preferred conformations of a number of stereoisomeric 2-(α-furyl) 1,3-dioxanes were established by PMR spectroscopy. It is shown that cis orientation of the NO2 groups with respect to the furyl ring is primarily realized for 2-(α'-nitro-α-furyl)-5-ethyl-5-nitro-1,3-dioxanes. © 1975 Plenum Publishing Corporation. |
|
dc.relation.ispartofseries |
Chemistry of Heterocyclic Compounds |
|
dc.title |
Research on furan acetal compounds - VII. PMR spectra, configuration, and conformations of substituted 2-(α-furyl)-1,3-diozanes |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
3 |
|
dc.relation.ispartofseries-volume |
10 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
276 |
|
dc.source.id |
SCOPUS00093122-1974-10-3-SID34250418334 |
|