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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 |