Cobalt-catalyzed tandem one-pot synthesis of polysubstituted imidazo[1,5-a]pyridines and imidazo[1,5-a]isoquinolines

dc.contributor.authorKumar, Anil
dc.date.accessioned2024-09-10T10:20:21Z
dc.date.available2024-09-10T10:20:21Z
dc.date.issued2022
dc.description.abstractAn efficient cobalt-catalyzed tandem one-pot method has been developed for the synthesis of polysubstituted imidazo[1,5-a]-N-heteroaromatics. The method involves Knoevenagel condensation followed by cobalt-catalyzed direct alkenylation to give the desired polysubstituted imidazo[1,5-a]pyridines and imidazo[1,5-a]isoquinolines in a one-pot manner. This method exhibits a broad substrate scope, provides moderate to good (39–74%) yields and is amenable to scale-up to the gram scale. An efficient cobalt-catalyzed tandem one-pot method has been developed for the synthesis of polysubstituted imidazo[1,5-a]-N-heteroaromatics.en_US
dc.identifier.urihttps://www.sciencedirect.com/org/science/article/abs/pii/S1477052022095957#!
dc.identifier.urihttps://dspace.bits-pilani.ac.in/xmlui/handle/123456789/15511
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectCobalt-catalyzeden_US
dc.titleCobalt-catalyzed tandem one-pot synthesis of polysubstituted imidazo[1,5-a]pyridines and imidazo[1,5-a]isoquinolinesen_US
dc.typeArticleen_US

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