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dc.creatorJovanović, Miloš
dc.creatorPetković, Miloš
dc.creatorJovanović, Predrag
dc.creatorSimić, Milena
dc.creatorTasić, Gordana
dc.creatorErić, Slavica
dc.creatorSavić, Vladimir
dc.date.accessioned2019-12-27T12:37:27Z
dc.date.available2019-12-27T12:37:27Z
dc.date.issued2020
dc.identifier.issn1434-193X
dc.identifier.urihttp://farfar.pharmacy.bg.ac.rs/handle/123456789/3481
dc.description.abstractAnnulations of allene-substituted proline derivatives promoted by transition metals have been investigated as a general way to access bicyclic structures with a bridgehead nitrogen. Two processes, Pd- and Ag-catalysed cyclisations, have been employed complementary to control the substitution pattern of the product. The investigated methodologies afforded the bicyclic derivatives in comparable yields, while Ag-catalysis showed higher level of diastereoselectivity. Both processes have been utilized in the synthesis of naturally occurring pyrroles longamide B, stylisine D and their derivatives.en
dc.publisherWiley-Blackwell
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172009/RS//
dc.rightsrestrictedAccess
dc.sourceEuropean Journal of Organic Chemistry
dc.subjectAg-catalysis
dc.subjectAnnulation
dc.subjectLongamide B
dc.subjectPd-catalysis
dc.subjectStylisine D
dc.titleProline Derived Bicyclic Derivatives through Metal Catalysed Cyclisations of Allenes: Synthesis of Longamide B, Stylisine D and their Derivativesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСавић, Владимир; Јовановић, Милош; Петковић, Милош; Јовановић, Предраг; Симић, Милена; Тасић, Гордана; Ерић, Славица;
dc.citation.volume2020
dc.citation.issue3
dc.citation.spage295
dc.citation.epage305
dc.citation.rankM21~
dc.identifier.wos000501722100001
dc.identifier.doi10.1002/ejoc.201901554
dc.identifier.scopus2-s2.0-85076378351
dc.type.versionpublishedVersion


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