Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/15589
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dc.contributor.authorDimitrijević, Mlađan-
dc.contributor.authorBogdanovic G.-
dc.contributor.authorTrifunović, Snežana-
dc.contributor.authorJoksović, Milan-
dc.date.accessioned2023-02-08T15:22:40Z-
dc.date.available2023-02-08T15:22:40Z-
dc.date.issued2023-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/15589-
dc.description.abstractAn efficient pTSA-mediated cyclization cascade reaction of Pfitzinger's ester and benzoyl hydrazines has been developed providing a simple procedure for synthesis of pyrrolo [3,4-c]quinoline-1,3-dione derivatives. Unlike traditional synthetic protocol, this method avoids an additional step of conversion of quinoline-3,4-dicarboxylic acids to an anhydride, allowing direct reaction of ester derivative with hydrazine nucleophiles.-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceTetrahedron-
dc.titleRapid access to pyrrolo[3,4-c]quinoline-1,3-diones: An improved synthetic protocol using a precursor prepared by Pfitzinger reaction-
dc.typearticle-
dc.identifier.doi10.1016/j.tet.2022.133236-
dc.identifier.scopus2-s2.0-85146062717-
Appears in Collections:Faculty of Science, Kragujevac

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