Stereochemical transformations of some seven-membered pyridoxine dimethyl ketals

dc.contributor.author	Petukhov A.
dc.contributor.author	Strel'nik A.
dc.contributor.author	Fedorenko V.
dc.contributor.author	Litvinov I.
dc.contributor.author	Lodochnikova O.
dc.contributor.author	Shtyrlin Y.
dc.contributor.author	Klimovitskii E.
dc.date.accessioned	2018-09-18T20:18:21Z
dc.date.available	2018-09-18T20:18:21Z
dc.date.issued	2007
dc.identifier.issn	1070-3632
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/138528
dc.description.abstract	According to the data of single crystal X-ray diffraction analysis and computational methods, the seven-membered rings of acylated pyridoxine acetonides have C 2 symmetry. Two stereochemical transformations in solutions, enantiotopomerization of P-, M-conformations with spiral chirality of twist-boat forms and diastereotopomerization of structures that differ in the configuration of the phenolic oxygen substituents, were revealed by dynamic 1H NMR spectroscopy. © 2007 Pleiades Publishing, Ltd.
dc.relation.ispartofseries	Russian Journal of General Chemistry
dc.title	Stereochemical transformations of some seven-membered pyridoxine dimethyl ketals
dc.type	Article
dc.relation.ispartofseries-issue	8
dc.relation.ispartofseries-volume	77
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1416
dc.source.id	SCOPUS10703632-2007-77-8-SID34848886354

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