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

dc.contributor.authorMandal, S.K.
dc.date.accessioned2020-12-18T08:18:08Z
dc.date.available2020-12-18T08:18:08Z
dc.date.issued2020
dc.descriptionOnly IISERM authors are available in the record.
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.identifier.citationAsian Journal of Organic Chemistry, 9(8), pp.1199-1204.en_US
dc.identifier.otherhttps://doi.org/10.1002/ajoc.202000239
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/abs/10.1002/ajoc.202000239
dc.identifier.urihttp://hdl.handle.net/123456789/3211
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.subjectC−H Activationen_US
dc.subjectTransition-metalsen_US
dc.subjectAcrylatesen_US
dc.subjectCatalysisen_US
dc.subjectCyclizationen_US
dc.titleIndazolone‐Assisted Sequential ortho‐Alkenylation‐Oxidative Aza‐Michael Addition of 1‐Arylindazolone Using Acrylates Under Ru(II) Catalysisen_US
dc.typeArticleen_US

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