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DC Field | Value | Language |
---|---|---|
dc.contributor.author | GHOSH, SOMNATH | en_US |
dc.contributor.author | MOHANTA, NIRMALA | en_US |
dc.contributor.author | GNANAPRAKASAM, BOOPATHY | en_US |
dc.date.accessioned | 2025-04-15T06:43:31Z | - |
dc.date.available | 2025-04-15T06:43:31Z | - |
dc.date.issued | 2024-08 | en_US |
dc.identifier.citation | European Journal of Organic Chemistry, 27(30). | en_US |
dc.identifier.issn | 1099-0690 | en_US |
dc.identifier.issn | 1434-193X | en_US |
dc.identifier.uri | https://doi.org/10.1002/ejoc.202400443 | en_US |
dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9468 | - |
dc.description.abstract | Herein, 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.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.subject | Copper catalyst | en_US |
dc.subject | Ring expansion | en_US |
dc.subject | Heterocycle | en_US |
dc.subject | Rearrangement | en_US |
dc.subject | Domino reaction | en_US |
dc.subject | 2024 | en_US |
dc.title | Cu-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 Azide | en_US |
dc.type | Article | en_US |
dc.contributor.department | Dept. of Chemistry | en_US |
dc.identifier.sourcetitle | European Journal of Organic Chemistry | en_US |
dc.publication.originofpublisher | Foreign | en_US |
Appears in Collections: | JOURNAL ARTICLES |
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