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dc.creatorStojanović, Milovan
dc.creatorMarković, Rade
dc.date.accessioned2019-01-30T17:21:13Z
dc.date.available2019-01-30T17:21:13Z
dc.date.issued2009
dc.identifier.issn0936-5214
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/580
dc.description.abstractSynthesis of new thiazolidine-fused five-, six-, and seven-membered heterocycles through vinylogous N-acyliminium ion-cyclization sequence, involving positions 3 and 4 of the thiazolidine ring, is described. The formation of bicyclic products, arising by generally disfavored 5-endo-trig cyclization initiated by sulfur atom acting as a nucleophile, indicates the preparative value of this method.en
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142007/RS//
dc.rightsrestrictedAccess
dc.sourceSynlett
dc.subjectCyclizationen
dc.subjectFused-ring systemsen
dc.subjectIminium ionsen
dc.subjectLactamsen
dc.subjectNeighboring-group effectsen
dc.titleSynthesis of the first thiazolidine-condensed five-, six-, and seven-membered heterocycles via cyclization of vinylogous N-acyliminium ionsen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСтојановић, Милован; Марковић, Р.;
dc.citation.issue12
dc.citation.spage1997
dc.citation.epage2001
dc.citation.other(12): 1997-2001
dc.citation.rankM22
dc.identifier.doi10.1055/s-0029-1217532
dc.identifier.rcubConv_4210
dc.identifier.scopus2-s2.0-67651208211
dc.identifier.wos000269337500023
dc.type.versionpublishedVersion


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