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

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DC Field	Value	Language
dc.contributor.author	Kumar, Anil	-
dc.date.accessioned	2024-09-10T10:20:21Z	-
dc.date.available	2024-09-10T10:20:21Z	-
dc.date.issued	2022	-
dc.identifier.uri	https://www.sciencedirect.com/org/science/article/abs/pii/S1477052022095957#!	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15511	-
dc.description.abstract	An 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.language.iso	en	en_US
dc.publisher	RSC	en_US
dc.subject	Chemistry	en_US
dc.subject	Cobalt-catalyzed	en_US
dc.title	Cobalt-catalyzed tandem one-pot synthesis of polysubstituted imidazo[1,5-a]pyridines and imidazo[1,5-a]isoquinolines	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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