Recent Developments in the Synthesis of Imidazo[1,2-a]pyridines

Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2864

Full metadata record

DC Field	Value	Language
dc.contributor.author	Kumar, Anil	-
dc.date.accessioned	2021-10-17T13:56:51Z	-
dc.date.available	2021-10-17T13:56:51Z	-
dc.date.issued	2015	-
dc.identifier.uri	https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0034-1380182	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2864	-
dc.description.abstract	Advances in the last decade for the synthesis of the imidazo[1,2-a]pyridine scaffold from various substrates employing approaches such as multicomponent reactions, tandem processes, rearrangement reactions, inter- and intramolecular oxidative/reductive cyclizations, and transition-metal-catalyzed C–H activation are summarized in this review. The mechanisms for the selected transformations are also discussed.	en_US
dc.language.iso	en	en_US
dc.publisher	Thieme	en_US
dc.subject	Chemistry	en_US
dc.subject	Imidazo[1,2-a]pyridine	en_US
dc.subject	2-aminopyridine	en_US
dc.subject	Tandem reaction	en_US
dc.subject	Multicomponent reaction	en_US
dc.subject	C–H activation	en_US
dc.title	Recent Developments in the Synthesis of Imidazo[1,2-a]pyridines	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

Files in This Item:

There are no files associated with this item.