dc.contributor.author |
Samitov Y. |
|
dc.contributor.author |
Yavorskii A. |
|
dc.contributor.author |
Gren' A. |
|
dc.contributor.author |
Bogat-skii A. |
|
dc.contributor.author |
Stepanova O. |
|
dc.date.accessioned |
2018-09-14T20:06:48Z |
|
dc.date.available |
2018-09-14T20:06:48Z |
|
dc.date.issued |
1975 |
|
dc.identifier.issn |
0009-3122 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/132140 |
|
dc.description.abstract |
2-Methyl-and 2,5-dialkyl-5-phenoxy-1,3-dioxanes were synthesized and separated into their geometrical isomers by precision rectification. The configuration and conformations of these isomers were determined by PMR spectroscopy. It is shown that the low-boiling trans isomers exist primarily in the chair conformation with an equatorial phenoxy group, whereas the high-boiling cis isomers exist primarily in the chair conformation with an axial phenoxy group. © 1976 Plenum Publishing Corporation. |
|
dc.relation.ispartofseries |
Chemistry of Heterocyclic Compounds |
|
dc.title |
Stereochemistry of heterocycles - XXXIX. Stereochemistry of 2-methyl-5-alkyl-5-phenoxy-1.3-dioxanes |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
8 |
|
dc.relation.ispartofseries-volume |
11 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
904 |
|
dc.source.id |
SCOPUS00093122-1975-11-8-SID34250393178 |
|