Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4985
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dc.contributor.authorAnsari, Arshad J.-
dc.date.accessioned2023-08-21T14:14:54Z-
dc.date.available2023-08-21T14:14:54Z-
dc.date.issued2022-
dc.identifier.citationOrganic and Biomolecular Chemistry, 20(23), 4746-4752.en_US
dc.identifier.urihttps://doi.org/10.1039/d2ob00467d-
dc.identifier.urihttp://hdl.handle.net/123456789/4985-
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractIn the current research, we envisaged the synthesis of bis-heterocycles containing the dihydroisoxazole ring by [3 + 2] cycloaddition of VECs (vinyl ethylene carbonates) and nitrile oxides, assisted by a Pd catalyst. Herein we explored hydroximoyl chlorides as versatile precursors for the in situ generation of nitrile oxides that were exploited to achieve the cycloaddition reaction on a vinyl group of VECs to generate bis-heterocycles. In silico-based studies of bis-heterocycles on the cyclooxygenase (COX) enzyme displayed selective COX-2 inhibition.en_US
dc.language.isoen_USen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectPd-Catalysed [3 + 2]-cycloadditionen_US
dc.subjectidentification of COX-2en_US
dc.subjectsilico analysisen_US
dc.titlePd-Catalysed [3 + 2]-cycloaddition towards the generation of bioactive bis-heterocycles/identification of COX-2 inhibitors via in silico analysisen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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