Iridium-catalyzed [4 + 2] annulation of 1-arylindazolones with α-diazo carbonyl compounds: access to indazolone-fused cinnolines

dc.contributor.authorMarkad, D.
dc.contributor.authorMandal, S.K.
dc.date.accessioned2020-11-25T11:11:35Z
dc.date.available2020-11-25T11:11:35Z
dc.date.issued2018
dc.descriptionOnly IISERM authors are available in the record.
dc.description.abstractAn efficient one-pot Ir-catalyzed method was developed for the synthesis of indazolone-fused cinnolines by [4 + 2] annulation of 1-arylindazolones with α-diazo carbonyl compounds via sequential C–H activation/carbene insertion/cyclization in a tandem manner. This method has excellent tolerance towards electron-withdrawing and electron-donating functional groups on 1-arylindazolone. This method was also found to be applicable to cyclic α-diazo carbonyl compounds.en_US
dc.identifier.citationOrganic and Biomolecular Chemistry, 16(44), pp. 8585-8595en_US
dc.identifier.otherhttps://doi.org/10.1039/C8OB01681J
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob01681j#!divAbstract
dc.identifier.urihttp://hdl.handle.net/123456789/2220
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectCarbonyl compoundsen_US
dc.subjectElectron-donatingen_US
dc.subjectActivation analysisen_US
dc.subjectIridiumen_US
dc.titleIridium-catalyzed [4 + 2] annulation of 1-arylindazolones with α-diazo carbonyl compounds: access to indazolone-fused cinnolinesen_US
dc.typeArticleen_US

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