Spatial structure of felodipine dissolved in DMSO by 1D NOE and 2D NOESY NMR spectroscopy

dc.contributor.author	Khodov I.
dc.contributor.author	Nikiforov M.
dc.contributor.author	Alper G.
dc.contributor.author	Blokhin D.
dc.contributor.author	Efimov S.
dc.contributor.author	Klochkov V.
dc.contributor.author	Georgi N.
dc.date.accessioned	2018-09-18T20:05:18Z
dc.date.available	2018-09-18T20:05:18Z
dc.date.issued	2013
dc.identifier.issn	0022-2860
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/136386
dc.description.abstract	Small organic molecules in dissolved state exist as an ensemble of conformers. In this work conformation of felodipine in dimethyl sulphoxide was studied and dominant stable conformers were determined. Effective interatomic distances were obtained by means of NOE spectroscopy. Fractions of different conformers were estimated by comparing effective distances and those obtained from quantum-chemical calculation [8]; averaging of distances was made following the N-site jump model. © 2012 Elsevier B.V. All rights reserved.
dc.relation.ispartofseries	Journal of Molecular Structure
dc.subject	Conformational analysis
dc.subject	Jump model
dc.subject	NOE
dc.subject	Nuclear magnetic resonance
dc.title	Spatial structure of felodipine dissolved in DMSO by 1D NOE and 2D NOESY NMR spectroscopy
dc.type	Article
dc.relation.ispartofseries-volume	1035
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	358
dc.source.id	SCOPUS00222860-2013-1035-SID84873579118

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Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.