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dc.creatorHusinec, Suren
dc.creatorMarković, Rade
dc.creatorPetković, Miloš
dc.creatorNasufović, Veselin
dc.creatorSavić, Vladimir
dc.date.accessioned2020-05-01T07:36:21Z
dc.date.available2020-05-01T07:36:21Z
dc.date.issued2011
dc.identifier.issn1523-7060
dc.identifier.urihttp://farfar.pharmacy.bg.ac.rs/handle/123456789/1527
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/3506
dc.description.abstractA base promoted cyclization of the protected N-propargylaminopyridines was shown to be an efficient method for the preparation of imidazo[1,2-a] pyridine derivatives. The reactions were carried out with a small excess of base, at room temperature or slightly above producing the heterocyclic products in moderate to good yields. The stereoelectronic properties of substituents on the pyridine ring were shown to influence the cyclization process.en
dc.publisherAmer Chemical Soc, Washington
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172009/RS//
dc.rightsrestrictedAccess
dc.sourceOrganic Letters
dc.titleA Base Promoted Cyclization of N-Propargylaminopyridines. Synthesis of Imidazo[1,2-a]pyridine Derivativesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСавић, Владимир; Хусинец, Сурен; Насуфовић, Веселин; Петковић, Милош; Марковић, Раде;
dc.citation.volume13
dc.citation.issue9
dc.citation.spage2286
dc.citation.epage2289
dc.citation.other13(9): 2286-2289
dc.citation.rankM21
dc.identifier.pmid21446664
dc.identifier.doi10.1021/ol200508x
dc.identifier.rcubconv_2419
dc.identifier.scopus2-s2.0-79955576570
dc.identifier.wos000289956700037
dc.type.versionpublishedVersion


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