Ruthenium-catalyzed (spiro)annulation of N-aryl-2,3-dihydrophthalazine-1,4-diones with quinones to access pentacyclic spiro-indazolones and fused-cinnolines

dc.contributor.authorMandal, Sanjay K.
dc.date.accessioned2023-08-16T09:20:49Z
dc.date.available2023-08-16T09:20:49Z
dc.date.issued2022
dc.descriptionOnly IISERM authors are available in the recorden_US
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.identifier.citationOrganic and Biomolecular Chemistry, 20(23), 4753-4764en_US
dc.identifier.urihttps://doi.org/10.1039/d2ob00493c
dc.identifier.urihttp://hdl.handle.net/123456789/4726
dc.language.isoen_USen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectN-aryl-2,3-dihydrophthalazine-1,4-dionesen_US
dc.subjectQuinonesen_US
dc.subjectFused-Cinnolinesen_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

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