dc.contributor.author |
Dimukhametov M. |
|
dc.contributor.author |
Ivkova G. |
|
dc.contributor.author |
Litvinov I. |
|
dc.contributor.author |
Fayzullin R. |
|
dc.contributor.author |
Mironov V. |
|
dc.date.accessioned |
2020-01-21T20:40:29Z |
|
dc.date.available |
2020-01-21T20:40:29Z |
|
dc.date.issued |
2019 |
|
dc.identifier.issn |
0959-9436 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/157587 |
|
dc.description.abstract |
© 2019 A mild approach to the synthesis of the title cage aminophosphonate has been developed based on the intramolecular cyclization of 2-(2-benzylideneaminoethoxy)-1-phenylbenzo[e]-1,3,2-azaoxaphosphorin-4-one obtained from 1-phenyl-2-chlorobenzo[e]-1,3,2-azaoxaphosphorin-4-one and (2-benzylideneaminoethoxy)trimethylsilane. The structure of isolated diastereomers of the product was determined by NMR spectroscopy and single crystal X-ray diffraction analysis. |
|
dc.relation.ispartofseries |
Mendeleev Communications |
|
dc.title |
Synthesis and structure of stereoisomers of 3,4-benzo-5,10-diphenyl-1,3-diaza-7-oxa-6-phosphabicyclo[4.3.1]decane-2,6-dione |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
2 |
|
dc.relation.ispartofseries-volume |
29 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
150 |
|
dc.source.id |
SCOPUS09599436-2019-29-2-SID85064314970 |
|