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Synthesis of the first thiazolidine-condensed five-, six-, and seven-membered heterocycles via cyclization of vinylogous N-acyliminium ions
dc.creator | Stojanović, Milovan | |
dc.creator | Marković, Rade | |
dc.date.accessioned | 2019-01-30T17:21:13Z | |
dc.date.available | 2019-01-30T17:21:13Z | |
dc.date.issued | 2009 | |
dc.identifier.issn | 0936-5214 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/580 | |
dc.description.abstract | Synthesis 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.relation | info:eu-repo/grantAgreement/MESTD/MPN2006-2010/142007/RS// | |
dc.rights | restrictedAccess | |
dc.source | Synlett | |
dc.subject | Cyclization | en |
dc.subject | Fused-ring systems | en |
dc.subject | Iminium ions | en |
dc.subject | Lactams | en |
dc.subject | Neighboring-group effects | en |
dc.title | Synthesis of the first thiazolidine-condensed five-, six-, and seven-membered heterocycles via cyclization of vinylogous N-acyliminium ions | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Стојановић, Милован; Марковић, Р.; | |
dc.citation.issue | 12 | |
dc.citation.spage | 1997 | |
dc.citation.epage | 2001 | |
dc.citation.other | (12): 1997-2001 | |
dc.citation.rank | M22 | |
dc.identifier.doi | 10.1055/s-0029-1217532 | |
dc.identifier.scopus | 2-s2.0-67651208211 | |
dc.identifier.wos | 000269337500023 | |
dc.type.version | publishedVersion |