dc.contributor.author |
Samitov Y. |
|
dc.contributor.author |
Garkovik N. |
|
dc.contributor.author |
Bogatskii A. |
|
dc.contributor.author |
Zolotareva S. |
|
dc.date.accessioned |
2018-09-14T20:06:05Z |
|
dc.date.available |
2018-09-14T20:06:05Z |
|
dc.date.issued |
1971 |
|
dc.identifier.issn |
0009-3122 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/132125 |
|
dc.description.abstract |
Six 2, 2, 5-trialkyl-5-α-alkoxyethyl-1, 3-dioxanes have been synthesized for the first time by the condensation of 2-alkyl-2-α-alkoxyethyl-1, 3-propane diols with ketones, and it has been shown by a study of their PMR spectra that they exist in the unsymmetrical boat conformation. The PMR spectra of a number of previously-synthesized 2-alkyl(aryl)-5-alkyl-5-α-alkoxyethyl-1, 3-dioxanes have been considered and it has been shown that from an analysis of the spectra it is possible to estimate the contents of geometrical isomers in a mixture. The stereochemistry of these compounds has been discussed. © 1971 Consultants Bureau. |
|
dc.relation.ispartofseries |
Chemistry of Heterocyclic Compounds |
|
dc.title |
Alkoxy compounds - XXII. Synthesis and PMR spectra of some 2-substituted 5-alkyl-5-α-alkoxyethyl-1,3-dioxanes |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
4 |
|
dc.relation.ispartofseries-volume |
4 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
448 |
|
dc.source.id |
SCOPUS00093122-1971-4-4-SID34250455787 |
|