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

dc.contributor.authorSakhuja, Rajeev
dc.date.accessioned2021-11-11T10:57:56Z
dc.date.available2021-11-11T10:57:56Z
dc.date.issued2021-01
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.urihttps://pubs.acs.org/doi/10.1021/acs.joc.0c02729
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3342
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectAnnulationsen_US
dc.subjectH2 Purificationen_US
dc.subjectOrganic compoundsen_US
dc.subjectColumn chromatographyen_US
dc.subjectEthanolen_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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