Structure and intramolecular lability of N-(thio)phosphoryl(thio)amides: XII. NMR study and computational modeling of the tautomeric forms of N-[dimethoxy(thio)phosphoryl]benzamides

dc.contributor.author	Karataeva F.
dc.contributor.author	Klochkov V.
dc.date.accessioned	2018-09-17T21:26:17Z
dc.date.available	2018-09-17T21:26:17Z
dc.date.issued	2005
dc.identifier.issn	1070-3632
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/134993
dc.description.abstract	The structure and intramolecular processes in solutions of N-(thio)phosphorylbenzamides were studied by means of 1H, 13C, and 31P NMR spectroscopy. Combined analysis of the NMR data and computational modeling gave evidence for the high lability of the compounds under study, that are capable of forming various tautomeric forms in solutions. The amide form with the NH proton arranged trans with respect to the C=O group was found to be preferred. ©2005 Pleiades Publishing, Inc.
dc.relation.ispartofseries	Russian Journal of General Chemistry
dc.title	Structure and intramolecular lability of N-(thio)phosphoryl(thio)amides: XII. NMR study and computational modeling of the tautomeric forms of N-[dimethoxy(thio)phosphoryl]benzamides
dc.type	Article
dc.relation.ispartofseries-issue	4
dc.relation.ispartofseries-volume	75
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	561
dc.source.id	SCOPUS10703632-2005-75-4-SID24644511664

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Публикации сотрудников КФУ Scopus [24551]
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