Reducing-Agent-Free Convergent Synthesis of Hydroxyimino-Decorated Tetracyclic Fused Cinnolines via RhIII-Catalyzed Annulation Using Nitroolefins

dc.contributor.authorMandal, Sanjay K.
dc.date.accessioned2023-08-22T11:17:24Z
dc.date.available2023-08-22T11:17:24Z
dc.date.issued2021
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractA mild Rh-catalyzed method was developed for the synthesis of hydroxyimino functionalized indazolo[1,2-a]cinnolines and phthalazino[2,3-a]cinnolines by reductive [4 + 2] annulation between 1-arylindazolones and 2-aryl-2,3-dihydrophthalazine-1,4-diones with varied nitroolefins. The targeted oxime decorated tetracyclic fused cinnolines were synthesized via sequential C–H activation/olefin insertion/reduction under reducing-agent-free conditions.en_US
dc.identifier.citationThe Journal of Organic Chemistry, 86(3), 2734–2747.en_US
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.joc.0c02729
dc.identifier.urihttp://hdl.handle.net/123456789/5022
dc.language.isoen_USen_US
dc.publisherACS Publicationsen_US
dc.subjectPurificationen_US
dc.subjectOrganic compoundsen_US
dc.titleReducing-Agent-Free Convergent Synthesis of Hydroxyimino-Decorated Tetracyclic Fused Cinnolines via RhIII-Catalyzed Annulation Using Nitroolefinsen_US
dc.typeArticleen_US

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