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Indazolone-Assisted Sequential ortho-Alkenylation-Oxidative Aza-Michael Addition of 1-Arylindazolone Using Acrylates Under Ru(II) Catalysis

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dc.contributor.author Sakhuja, Rajeev
dc.date.accessioned 2021-11-11T10:58:08Z
dc.date.available 2021-11-11T10:58:08Z
dc.date.issued 2020-06-12
dc.identifier.uri https://onlinelibrary.wiley.com/doi/abs/10.1002/ajoc.202000239
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3345
dc.description.abstract A 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.iso en en_US
dc.publisher Wiley en_US
dc.subject Chemistry en_US
dc.subject Indazolone-Assisted en_US
dc.title Indazolone-Assisted Sequential ortho-Alkenylation-Oxidative Aza-Michael Addition of 1-Arylindazolone Using Acrylates Under Ru(II) Catalysis en_US
dc.type Article en_US


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