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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/15569
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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2024-09-13T08:57:28Z-
dc.date.available2024-09-13T08:57:28Z-
dc.date.issued2022-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2022/ob/d2ob00493c-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15569-
dc.description.abstractRu(II)-catalyzed strategies were developed for the [4 + 1] and [4 + 2] oxidative coupling between N-aryl-2,3-dihydrophthalazine-1,4-diones and 1,4-benzoquinones, achieving spiro-indazolones and fused-cinnolines, respectively. Mild, aerobic and external oxidant-free conditions, as well as the use of a ruthenium catalyst for such (spiro)annulative strategies with quinones over reported Rh/Ir-catalyts, underline the rewards of the disclosed protocols.en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectFused-cinnolinesen_US
dc.subjectRuthenium-catalyzeden_US
dc.titleRuthenium-catalyzed (spiro)annulation of N-aryl-2,3-dihydrophthalazine-1,4-diones with quinones to access pentacyclic spiro-indazolones and fused-cinnolinesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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