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

Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/8823

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DC Field	Value	Language
dc.rights.license	BY-NC-ND	-
dc.contributor.author	Bugarinović, Jovana	-
dc.contributor.author	Bogdanovic, Goran A.	-
dc.contributor.author	Damljanović, Ivan	-
dc.date.accessioned	2020-09-19T16:46:41Z	-
dc.date.available	2020-09-19T16:46:41Z	-
dc.date.issued	2017	-
dc.identifier.issn	0936-5214	-
dc.identifier.uri	https://scidar.kg.ac.rs/handle/123456789/8823	-
dc.description.abstract	© Georg Thieme VerlagStuttgart · New York. Aluminum 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.	-
dc.rights	openAccess	-
dc.rights.uri	https://creativecommons.org/licenses/by-nc-nd/4.0/	-
dc.source	Synlett	-
dc.title	Acid-Catalyzed [3+2] Cycloaddition of Enones with Azomethine Imines for Easy Access to Tetrahydropyrazolopyrazolones	-
dc.type	article	-
dc.identifier.doi	10.1055/s-0036-1588678	-
dc.identifier.scopus	2-s2.0-85006416108	-
Appears in Collections:	Faculty of Science, Kragujevac

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