Chloroform as a carbon monoxide source in palladium-catalyzed synthesis of 2-amidoimidazo [1,2-a]pyridines

Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3273

Full metadata record

DC Field	Value	Language
dc.contributor.author	Nitha, P R	-
dc.contributor.author	Manu, M	-
dc.contributor.author	Joseph	-
dc.contributor.author	Greeshma, Gopalan	-
dc.contributor.author	Maiti, K K	-
dc.contributor.author	Radhakrishnan, K V	-
dc.contributor.author	Das, Parthasarathi	-
dc.date.accessioned	2018-10-15T11:19:00Z	-
dc.date.available	2018-10-15T11:19:00Z	-
dc.date.issued	2018-08	-
dc.identifier.citation	Organic & Biomolecular Chemistry, 16(35):6430–6437	en_US
dc.identifier.uri	http://10.10.100.66:8080/xmlui/handle/123456789/3273	-
dc.description.abstract	A palladium-catalyzed aminocarbonylation strategy exploiting chloroform as a CO source has been developed for the synthesis of biologically potent 2-amidoimidazopyridine scaffolds. The aminocarbonylation reaction was found to be general with a range of amines and substituted imidazopyridines. Preliminary biological evaluation of cytotoxicity on selected examples provides scope for future investigations.	en_US
dc.language.iso	en	en_US
dc.publisher	The Royal Society of Chemistry	en_US
dc.title	Chloroform as a carbon monoxide source in palladium-catalyzed synthesis of 2-amidoimidazo [1,2-a]pyridines	en_US
dc.type	Article	en_US
Appears in Collections:	2018

Files in This Item:

File	Description	Size	Format
Chloroform as a carbon-P. R. Nitha-Organic & Biomolecular Chemistry.pdf Restricted Access		1.2 MB	Adobe PDF	View/Open Request a copy

DSpace JSPUI