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

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dc.contributor.authorKumar, Anil
dc.date.accessioned2021-10-14T13:10:33Z
dc.date.available2021-10-14T13:10:33Z
dc.date.issued2019-08
dc.description.abstractAn 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.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040403919306884?via%3Dihub
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2819
dc.language.isoenen_US
dc.publisherElsieveren_US
dc.subjectChemistryen_US
dc.subjectMetal-freeen_US
dc.subjectTandem reactionen_US
dc.subjectPyridyl ureaen_US
dc.titleMetal-free synthesis of pyridin-2-yl ureas from 2-aminopyridinium saltsen_US
dc.typeArticleen_US

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