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 |