Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1787
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dc.contributor.authorMandal, S.K.-
dc.date.accessioned2020-11-18T09:05:58Z-
dc.date.available2020-11-18T09:05:58Z-
dc.date.issued2018-
dc.identifier.citationJournal of Organic Chemistry, 83(19), pp. 11661-11673.en_US
dc.identifier.other10.1021/acs.joc.8b01630.-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.joc.8b01630-
dc.identifier.urihttp://hdl.handle.net/123456789/1787-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractA Rh(III)-catalyzed strategy involving the [4+1] annulation of 2-arylphthalazine-1,4-diones with α-diazo carbonyl compounds was developed, accessing a series of unprecedented hydroxy-dihydroindazolo-fused phthalazines in good to excellent yields. By varying the additive, phthalazino-fused cinnolines were synthesized under Rh-catalyzed conditions via [4+2] annulation between the same starting materials. Notably, such two strategies showed a good functional group tolerance and high atom efficiency.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectCarbonyl compoundsen_US
dc.subjectDiazo carbonyl compoundsen_US
dc.subjectPhthalazinesen_US
dc.subjectRhodium compoundsen_US
dc.subjectCatalysisen_US
dc.subjectAtom efficiencyen_US
dc.titleAdditive-Driven Rhodium-Catalyzed [4+1]/[4+2] Annulations of N-Arylphthalazine-1,4-dione with α-Diazo Carbonyl Compoundsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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