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dc.creatorSimić, Milena
dc.creatorJovanović, Predrag
dc.creatorPetković, Miloš
dc.creatorTasić, Gordana
dc.creatorJovanović, Miloš
dc.creatorSavić, Vladimir
dc.date.accessioned2021-06-08T10:21:43Z
dc.date.available2021-06-08T10:21:43Z
dc.date.issued2021
dc.identifier.issn0022-152X
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/3908
dc.description.abstractOctahydro-dipyrroloquinoline skeleton is the building component of a very few naturally occurring compounds. Nevertheless, these natural products have been attractive synthetic targets, and their study commanded development of efficient synthesis of this core. While the reported methods are based on the dimerization procedure of N-arylpyrrolidines of N-arylhomopropargyl amines, our approach relay on dipolar cycloaddition/amination sequence. This strategic approach allows sequential introduction of aromatic moieties increasing the product diversity and hence may be useful in further exploration of incargranine B or seneciobipyrrolidine derivatives.
dc.publisherWiley, HeteroCorporation
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200161/RS//
dc.relationFP7 RegPot project FCUB ERA GA No. 256716
dc.rightsrestrictedAccess
dc.sourceJournal of Heterocyclic Chemistry
dc.titleToward the synthesis of incargranine B and seneciobipyrrolidine. Synthesis of octahydro-dipyrroloquinoline skeleton via dipolar cycloaddition/amination sequence
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСимић, Милена; Јовановић, Предраг; Петковић, Милош; Јовановић, Милош; Савић, Владимир; Тасић, Гордана;
dc.citation.rankM22
dc.identifier.wos000654632400001
dc.identifier.doi10.1002/jhet.4303
dc.identifier.scopus2-s2.0-85106458850
dc.type.versionpublishedVersion


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Приказ основних података о документу