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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3345
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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2021-11-11T10:58:08Z-
dc.date.available2021-11-11T10:58:08Z-
dc.date.issued2020-06-12-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/abs/10.1002/ajoc.202000239-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3345-
dc.description.abstractA one-pot annulation of 1-arylindazolones and acrylates is achieved through Ru(II)-catalyzed sequential ortho-alkenylation followed by oxidative intramolecular aza-Michael addition reaction to deliver substituted indazolo[1,2-a]indazolylidenes in good-to-excellent yields. The strategy showcased high functional group tolerance and the directing group ability of indazolone moiety was established for Csp2-H bond activation.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectIndazolone-Assisteden_US
dc.titleIndazolone-Assisted Sequential ortho-Alkenylation-Oxidative Aza-Michael Addition of 1-Arylindazolone Using Acrylates Under Ru(II) Catalysisen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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