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dc.creatorJovanović, Miloš
dc.creatorSimić, Milena
dc.creatorPetković, Miloš
dc.creatorTasić, Gordana
dc.creatorMaslak, Veselin
dc.creatorJovanović, Predrag
dc.creatorSavić, Vladimir
dc.date.accessioned2022-06-16T09:53:48Z
dc.date.available2022-06-16T09:53:48Z
dc.date.issued2022
dc.identifier.issn0022-152X
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/4175
dc.description.abstractA 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.publisherWiley Periodicals LLC
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200161/RS//
dc.rightsrestrictedAccess
dc.sourceJournal of Heterocyclic Chemistry
dc.titleHighly exo selective, photochemically promoted cyclization of iodoallene derivatives
dc.typearticle
dc.rights.licenseARR
dc.citation.volume59
dc.citation.issue8
dc.citation.spage1435
dc.citation.epage1440
dc.citation.rankM22
dc.identifier.wos000766376800001
dc.identifier.doi10.1002/jhet.4472
dc.identifier.scopus2-s2.0-85125948339
dc.type.versionpublishedVersion


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