Stereochemistry of organophosphorus compounds - Communication 8. Configuration and conformational mobility of trans-2,3-diphenyl-4-dimethoxyphosphonoisoxazolidine ring

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

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