dc.creator | Jovanović, Predrag | |
dc.creator | Petković, Miloš | |
dc.creator | Ivković, Branka | |
dc.creator | Savić, Vladimir | |
dc.date.accessioned | 2019-09-02T11:55:26Z | |
dc.date.available | 2019-09-02T11:55:26Z | |
dc.date.issued | 2016 | |
dc.identifier.issn | 0957-4166 | |
dc.identifier.uri | https://farfar.pharmacy.bg.ac.rs/handle/123456789/2723 | |
dc.description.abstract | Structural variations of the heterocyclic ring of the recently introduced pyrrolidine derived thiourea organocatalysts have been studied. The results showed that the stereoselectivity is highly dependent on the substitution pattern reaching a moderate level, while the yields were generally less influenced by the structural changes. The outlined results may be helpful in further exploration of the thiourea catalyst represented by structure II. | en |
dc.publisher | Pergamon-Elsevier Science Ltd, Oxford | |
dc.relation | info:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172009/RS// | |
dc.rights | restrictedAccess | |
dc.source | Therapeutic Advances in Drug Safety | |
dc.title | Pyrrolidine derived thioureas as organocatalysts in the Michael reaction of vinyl sulfone. Structure-stereoselectivity study | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Петковић, Милош; Ивковић, Бранка; Савић, Владимир; Јовановић, Предраг; | |
dc.citation.volume | 27 | |
dc.citation.issue | 19 | |
dc.citation.spage | 990 | |
dc.citation.epage | 997 | |
dc.citation.other | 27(19): 990-997 | |
dc.citation.rank | M22 | |
dc.identifier.wos | 000383817100012 | |
dc.identifier.doi | 10.1016/j.tetasy.2016.08.004 | |
dc.identifier.scopus | 2-s2.0-84984982209 | |
dc.type.version | publishedVersion | |