| dc.contributor.author |
Kumar, Indresh |
|
| dc.date.accessioned |
2024-09-12T04:10:42Z |
|
| dc.date.available |
2024-09-12T04:10:42Z |
|
| dc.date.issued |
2023-07 |
|
| dc.identifier.uri |
https://pubs.acs.org/doi/10.1021/acs.joc.3c01092 |
|
| dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15541 |
|
| dc.description.abstract |
A straightforward method has been developed to synthesize 2-aryl-3-(2-aminoaryl) quinoxalines from 2-arylindoles and 1,2-diaminoarenes under mild electrochemical conditions. The reaction proceeds through in situ generations of 2-arylindole-3-ones under electrochemical oxidative dearomatization of 2-arylindoles, followed by a ring opening-cyclization sequence with 1,2-diaminoarenes. A series of 2-aryl-3-(2-aminoaryl) quinoxalines have been prepared with moderate to good yields (up to 75%). |
en_US |
| dc.language.iso |
en |
en_US |
| dc.publisher |
ACS |
en_US |
| dc.subject |
Chemistry |
en_US |
| dc.subject |
Atmospheric chemistry |
en_US |
| dc.subject |
Electrochemical synthesis |
en_US |
| dc.subject |
Electrodes |
en_US |
| dc.subject |
Fossil fuels |
en_US |
| dc.subject |
Purification |
en_US |
| dc.title |
Electrochemical Synthesis of 2-Aryl-3-(2-aminoaryl)quinoxalines via Oxidative Dearomatization/Ring-Opening/Cyclization Cascade Sequence of 2-Arylindoles with 1,2-Diaminoarenes |
en_US |
| dc.type |
Article |
en_US |