Приказ основних података о документу

dc.creatorRašović, Aleksandar
dc.creatorSteel, Peter J.
dc.creatorKleinpeter, Erich
dc.creatorMarković, Rade
dc.date.accessioned2021-02-24T09:46:30Z
dc.date.available2021-02-24T09:46:30Z
dc.date.issued2007
dc.identifier.issn0040-4020
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4255
dc.description.abstractA new synthetic approach to 2,3-dihydro-4H-1,3-thiazine derivatives based upon reductive rearrangement of 1,2-dithiole-3-ylidene thiones has been developed. In turn, the 1,2-dithiole derivatives were prepared by an efficient ring-opening-closing process of 2-alkylidene-4-oxothiazolidines, induced in the presence of Lawesson's reagent by intramolecular non-bonded 1,5-type S⋯O interactions in the 4-oxothiazolidine precursors.sr
dc.language.isoensr
dc.publisherElseviersr
dc.relationThe Ministry of Science, Technology and Development of the Republic of Serbia, grant no. 1709sr
dc.relation.isversionofhttps://cer.ihtm.bg.ac.rs/handle/123456789/4587
dc.relation.isreferencedbyhttps://cer.ihtm.bg.ac.rs/handle/123456789/4588
dc.relation.isreferencedbyhttps://cer.ihtm.bg.ac.rs/handle/123456789/4589
dc.rightsrestrictedAccesssr
dc.sourceTetrahedronsr
dc.subject1,2-Dithiolessr
dc.subject1,3-Thiazinessr
dc.subjectNon-bonded S⋯O interactionsr
dc.subjectRearrangementsr
dc.subjectThiazolidinessr
dc.titleRegioselective synthesis of 1,3-thiazines by sequential 4-oxothiazolidine to 1,2-dithiole to 1,3-thiazine transformations: role of intramolecular non-bonded S/O interactionssr
dc.typearticlesr
dc.rights.licenseARRsr
dcterms.abstractМарковић, Раде; Рашовић, Aлександар; Стеел, Петер Ј.; Клеинпетер, Ерицх;
dc.citation.volume63
dc.citation.issue9
dc.citation.spage1937
dc.citation.epage1945
dc.citation.rankM21
dc.description.otherPeer-reviewed version: [https://cer.ihtm.bg.ac.rs/handle/123456789/4587]
dc.description.otherCrystallographic data (CCDC 607823): [https://cer.ihtm.bg.ac.rs/handle/123456789/4588]
dc.description.otherCrystallographic data (CCDC 607824): [https://cer.ihtm.bg.ac.rs/handle/123456789/4589]
dc.identifier.doi10.1016/j.tet.2006.12.075
dc.identifier.scopus2-s2.0-33846417967
dc.identifier.wos000244406500007
dc.type.versionpublishedVersionsr


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