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Highly exo selective, photochemically promoted cyclization of iodoallene derivatives
dc.creator | Jovanović, Miloš | |
dc.creator | Simić, Milena | |
dc.creator | Petković, Miloš | |
dc.creator | Tasić, Gordana | |
dc.creator | Maslak, Veselin | |
dc.creator | Jovanović, Predrag | |
dc.creator | Savić, Vladimir | |
dc.date.accessioned | 2022-06-16T09:53:48Z | |
dc.date.available | 2022-06-16T09:53:48Z | |
dc.date.issued | 2022 | |
dc.identifier.issn | 0022-152X | |
dc.identifier.uri | https://farfar.pharmacy.bg.ac.rs/handle/123456789/4175 | |
dc.description.abstract | A photochemically promoted intramolecular cyclization of aryl-, vinyl-, and alkyliodo allenes has been developed. The optimal conditions employed [Ir(ppy)2(dtbbpy)]PF6 (1 mol%) as catalyst affording products with high exo selectivity in moderate to good yields. Chiral substrates showed diastereoselectivity of up to 95/5 favoring trans product. | |
dc.publisher | Wiley Periodicals LLC | |
dc.relation | info:eu-repo/grantAgreement/MESTD/inst-2020/200161/RS// | |
dc.rights | restrictedAccess | |
dc.source | Journal of Heterocyclic Chemistry | |
dc.title | Highly exo selective, photochemically promoted cyclization of iodoallene derivatives | |
dc.type | article | |
dc.rights.license | ARR | |
dc.citation.volume | 59 | |
dc.citation.issue | 8 | |
dc.citation.spage | 1435 | |
dc.citation.epage | 1440 | |
dc.citation.rank | M22 | |
dc.identifier.wos | 000766376800001 | |
dc.identifier.doi | 10.1002/jhet.4472 | |
dc.identifier.scopus | 2-s2.0-85125948339 | |
dc.type.version | publishedVersion |