Copper and palladium-catalyzed sequential reactions: one-pot synthesis of isoindolo[2,1-b]isoquinolin-7(5H)-ones

dc.contributor.authorKumar, Anil
dc.date.accessioned2021-10-14T13:10:55Z
dc.date.available2021-10-14T13:10:55Z
dc.date.issued2019
dc.description.abstractA highly efficient protocol has been developed for the synthesis of diversely substituted isoindolo[2,1-b]isoquinolin-7(5H)-ones through sequential Cu(II)-catalyzed Sonogashira coupling, intramolecular hydroamidation followed by palladium-catalyzed ligand-free Heck reaction. Good to excellent yields (41–94%) were observed with excellent substrate scope and functional group tolerance. The developed method represents a practical strategy for the construction of bioactive isoindolo[2,1-b]isoquinolin-7(5H)-ones.en_US
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2019/ob/c9ob00440h
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2821
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectCopperen_US
dc.subjectPalladium-catalyzeden_US
dc.subjectIsoindoloen_US
dc.titleCopper and palladium-catalyzed sequential reactions: one-pot synthesis of isoindolo[2,1-b]isoquinolin-7(5H)-onesen_US
dc.typeArticleen_US

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