dc.contributor.author |
Arbuzov B. |
|
dc.contributor.author |
Kataev V. |
|
dc.contributor.author |
Arshinova R. |
|
dc.contributor.author |
Gubaidullin R. |
|
dc.date.accessioned |
2018-09-20T20:41:31Z |
|
dc.date.available |
2018-09-20T20:41:31Z |
|
dc.date.issued |
1978 |
|
dc.identifier.issn |
0568-5230 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/146181 |
|
dc.description.abstract |
1. In solution, 5,5-bis(bromomethyl)-1,3,2-dioxaphosphorinane exists as an equilibrium mixture of conformera with trans-gauche and gauche-gauche orientations of the Br-C-C5-C-Br chain (the first index refers to the equatorial halomethyl group). 2. The 2-chloro- and 2-ethoxy-5,t-bis(chloromethyl)-1,3,2,-dioxaphosphorinanes exist not only in the trans-gauche and gauche-gauche forms but also in a gauche-trans form with the C-Cl bond of the axial chloromethyl group in trans orientation. 3. 2-Hydro-2-oxo-5,5-bis(halomethyl)-1,3,2-dioxaphosphorinanes exist as mixtures of conformers containing two chair forms with axial and equatorial phosphoryl groups. © 1979 Plenum Publishing Corporation. |
|
dc.relation.ispartofseries |
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science |
|
dc.title |
The geometrical structures of phosphorus-containing heterocycles 20. 1,3,2-Dioxaphosphorinanes with two geminal axes of internal rotation |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
11 |
|
dc.relation.ispartofseries-volume |
27 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
2179 |
|
dc.source.id |
SCOPUS05685230-1978-27-11-SID34250286699 |
|