dc.contributor.author |
Arbuzov B. |
|
dc.contributor.author |
Samitov Y. |
|
dc.contributor.author |
Dianova E. |
|
dc.contributor.author |
Lisin A. |
|
dc.date.accessioned |
2018-09-14T20:30:04Z |
|
dc.date.available |
2018-09-14T20:30:04Z |
|
dc.date.issued |
1975 |
|
dc.identifier.issn |
0568-5230 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/132529 |
|
dc.description.abstract |
1. The 1,3-bipolar cycloaddition of dimethyl vinylphosphonate to C,N-diphenylnitrone gave trans-2,3-diphenyl-4-dimethoxyphosphonoisoxazolidine, the structure and configurations of which were proved via the1H and31P NMR,1H -{31P} NMDR, and IR spectra. 2. From the stereospecificity of the vicinal spin-spin coupling constants3JPCCH and3JHCCH and the temperature dependence of the NMR spectra it follows that the isoxazolidine ring is found in the pseudorotation state. © 1975 Plenum Publishing Corporation. |
|
dc.relation.ispartofseries |
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science |
|
dc.title |
Stereochemistry of organophosphorus compounds - Communication 8. Configuration and conformational mobility of trans-2,3-diphenyl-4-dimethoxyphosphonoisoxazolidine ring |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
4 |
|
dc.relation.ispartofseries-volume |
24 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
823 |
|
dc.source.id |
SCOPUS05685230-1975-24-4-SID33646727607 |
|