| 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 |