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Acid-Catalyzed [3+2] Cycloaddition of Enones with Azomethine Imines for Easy Access to Tetrahydropyrazolopyrazolones

dc.creatorJovanović, Jovana P.
dc.creatorBogdanović, Goran A.
dc.creatorDamljanović, Ivan S.
dc.date.accessioned2018-03-01T17:18:44Z
dc.date.available2018-03-01T17:18:44Z
dc.date.issued2017
dc.identifier.issn0936-5214
dc.identifier.issn1437-2096
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/1359
dc.description.abstractAluminum chloride (AlCl3) or zirconium chloride (ZrCl4) catalyzes efficiently the [3+2] cycloaddition of N, N-cyclic azomethine imines with enones which contain the vinyl group. The scope of the reaction towards various azomethine imines and enones has been explored. Access to diastereomerically pure 6-acyl-5-aryltetrahydropyrazolo[1,2-a] pyrazol-1(5H)-ones is provided by easy chromatographic separations.en
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172034/RS//
dc.rightsrestrictedAccessen
dc.sourceSynletten
dc.subjectdipolar cycloadditionen
dc.subjectN,N -cyclic azomethine imineen
dc.subjectenoneen
dc.subjectN,N -bicyclic heterocyclesen
dc.subjectLewis aciden
dc.titleAcid-Catalyzed [3+2] Cycloaddition of Enones with Azomethine Imines for Easy Access to Tetrahydropyrazolopyrazolonesen
dc.typearticleen
dcterms.abstractЈовановиц, Јована П.; Богдановић Горан; Дамљановиц, Иван;
dc.citation.volume28
dc.citation.issue6
dc.citation.spage664
dc.citation.epage668
dc.identifier.wos000402749400010
dc.identifier.doi10.1055/s-0036-1588678
dc.citation.otherArticle Number: UNSP st-2016-b0542-l
dc.citation.rankM22
dc.type.versionpublishedVersion
dc.identifier.scopus2-s2.0-85006416108


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