Metal-free synthesis of pyridin-2-yl ureas from 2-aminopyridinium salts

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DC Field	Value	Language
dc.contributor.author	Kumar, Anil	-
dc.date.accessioned	2021-10-14T13:10:33Z	-
dc.date.available	2021-10-14T13:10:33Z	-
dc.date.issued	2019-08	-
dc.identifier.uri	https://www.sciencedirect.com/science/article/pii/S0040403919306884?via%3Dihub	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2819	-
dc.description.abstract	An unprecedented base promoted domino approach has been developed for the synthesis of pyridin-2-yl urea derivatives via the reaction of 2-aminopyridinium salts and arylamines. The developed strategy tolerated a wide range of functional groups and afforded pyridin-2-yl ureas in moderate to good yields. The reaction was postulated to involve tandem cyclization, intermolecular nucleophilic addition, ring opening, and demethylation.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsiever	en_US
dc.subject	Chemistry	en_US
dc.subject	Metal-free	en_US
dc.subject	Tandem reaction	en_US
dc.subject	Pyridyl urea	en_US
dc.title	Metal-free synthesis of pyridin-2-yl ureas from 2-aminopyridinium salts	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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