Dynamic NMR study of cyclic derivatives of pyridoxine

dc.contributor.author	Rakhmatullin I.
dc.contributor.author	Galiullina L.
dc.contributor.author	Garipov M.
dc.contributor.author	Strel'nik A.
dc.contributor.author	Shtyrlin Y.
dc.contributor.author	Klochkov V.
dc.date.accessioned	2018-09-18T20:09:41Z
dc.date.available	2018-09-18T20:09:41Z
dc.date.issued	2014
dc.identifier.issn	0749-1581
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/137125
dc.description.abstract	A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spectroscopy (NOESY) NMR. The free energies of activation for the pyridyl-oxygen rotation of the 2,4-dinitrophenyl ether of the seven-membered acetals of pyridoxine were measured by dynamic NMR. A conformational exchange between the chair and twist forms of the seven-membered acetal ring was confirmed by dynamic NMR and STO3G computations. © 2014 John Wiley & Sons, Ltd.
dc.relation.ispartofseries	Magnetic Resonance in Chemistry
dc.subject	Dynamic 1H NMR
dc.subject	Energy barrier
dc.subject	Pyridoxine
dc.title	Dynamic NMR study of cyclic derivatives of pyridoxine
dc.type	Article in Press
dc.collection	Публикации сотрудников КФУ
dc.source.id	SCOPUS07491581-2014-SID84906034662

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