| dc.contributor.author | Kumar, Indresh | |
| dc.date.accessioned | 2024-09-12T04:19:25Z | |
| dc.date.available | 2024-09-12T04:19:25Z | |
| dc.date.issued | 2022-11 | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/acs.joc.2c01734 | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15544 | |
| dc.description.abstract | An electrochemical method has been developed to synthesize 2,2-disubstituted indolin-3-ones under mild conditions. A series of nucleophiles have been added to the 2-arylindole-3-ones, generated in situ under metal-free electrochemical oxidative dearomatization of 2-arylindoles, to afford 2,2-disubstituted 3-carbonyl indoles with heteroquaternary centers in 57–79% yields. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | ACS | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Electrodes | en_US |
| dc.subject | Fossil fuels | en_US |
| dc.subject | Indoles | en_US |
| dc.subject | Substitution reactions | en_US |
| dc.title | Electrochemical Oxidative Addition of Nucleophiles on 2-Arylindoles: Synthesis of C2-Heteroquaternary Indolin-3-ones | en_US |
| dc.type | Article | en_US |
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