Acylated benzothiazinesulfoneamides: Synthesis and molecular structure

dc.contributor.author	Tevs O.
dc.contributor.author	Veremeichik Y.
dc.contributor.author	Shurpik D.
dc.contributor.author	Lodochnikova O.
dc.contributor.author	Plemenkov V.
dc.date.accessioned	2018-09-19T21:00:35Z
dc.date.available	2018-09-19T21:00:35Z
dc.date.issued	2016
dc.identifier.issn	1070-3632
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/143507
dc.description.abstract	© 2016, Pleiades Publishing, Ltd.1,2,3,4,4a,10b-Hexahydro-1,4-methano-6H-dibenzo[c,e]-5,6-thiazine-5,5-dioxide has been converted into the corresponding N-acyl derivatives via the reaction with acid chlorides and anhydrides. X-Ray diffraction data have revealed the presence of an intramolecular С–H···O=S hydrogen bond in the molecules of the obtained compounds.
dc.relation.ispartofseries	Russian Journal of General Chemistry
dc.subject	acylation
dc.subject	intramolecular interactions
dc.subject	sulfonamides
dc.subject	X-ray diffraction analysis
dc.title	Acylated benzothiazinesulfoneamides: Synthesis and molecular structure
dc.type	Article
dc.relation.ispartofseries-issue	8
dc.relation.ispartofseries-volume	86
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1850
dc.source.id	SCOPUS10703632-2016-86-8-SID84988850933

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