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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3352
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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2021-11-11T10:58:36Z-
dc.date.available2021-11-11T10:58:36Z-
dc.date.issued2018-09-05-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.joc.8b01630-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3352-
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.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectAdditivesen_US
dc.subjectAddition reactionsen_US
dc.subjectMixturesen_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:Department of Chemistry

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