Показать сокращенную информацию
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 |