Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9468
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dc.contributor.authorGHOSH, SOMNATHen_US
dc.contributor.authorMOHANTA, NIRMALAen_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2025-04-15T06:43:31Z-
dc.date.available2025-04-15T06:43:31Z-
dc.date.issued2024-08en_US
dc.identifier.citationEuropean Journal of Organic Chemistry, 27(30).en_US
dc.identifier.issn1099-0690en_US
dc.identifier.issn1434-193Xen_US
dc.identifier.urihttps://doi.org/10.1002/ejoc.202400443en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9468-
dc.description.abstractHerein, we report a novel and efficient method for the synthesis of new class of 5-oxo-5,6-dihydro-[1,2,3]triazolo[1,5-c]quinazoline derivatives by copper-catalyzed reaction of α, β-unsaturated keto/ester methyleneindolinone with sodium azide at room temperature via an azide-alkene cyclization and ring expansion rearrangement. This method is applicable to a variety of α, β-unsaturated keto/ester methyleneindolinone and displayed wide functional group tolerance.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectCopper catalysten_US
dc.subjectRing expansionen_US
dc.subjectHeterocycleen_US
dc.subjectRearrangementen_US
dc.subjectDomino reactionen_US
dc.subject2024en_US
dc.titleCu-Catalyzed Synthesis of [1,2,3]triazolo[1,5-c]quinazolin-5(6H)-one Derivatives via Sequential Reaction of Ethyl-2-(2-oxoindolin-3-ylidene)acetate with Sodium Azideen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleEuropean Journal of Organic Chemistryen_US
dc.publication.originofpublisherForeignen_US
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