dc.contributor.author |
Kumar, Anil |
|
dc.date.accessioned |
2024-09-10T09:21:13Z |
|
dc.date.available |
2024-09-10T09:21:13Z |
|
dc.date.issued |
2021-02 |
|
dc.identifier.uri |
https://pubs.acs.org/doi/full/10.1021/acs.orglett.3c00240 |
|
dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15507 |
|
dc.description.abstract |
A copper(II)-catalyzed cascade synthesis of 1H-pyrrolo[3,4-b]quinoline-1,3(2H)-diones has been achieved from readily available o-amino carbonyl compounds and maleimides. This one-pot cascade strategy involves a copper-catalyzed aza-Michael addition followed by condensation and oxidation to deliver the target molecules. The protocol features a broad substrate scope and excellent functional group tolerance and affords products in moderate to good (44–88%) yields. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
ACS |
en_US |
dc.subject |
Chemistry |
en_US |
dc.subject |
Quinoline |
en_US |
dc.subject |
Synthesis |
en_US |
dc.title |
Copper(II)-Catalyzed Synthesis of Pyrrolo[3,4-b]quinolinediones from o-Amino Carbonyl Compounds and Maleimides |
en_US |
dc.type |
Article |
en_US |