Visible light triggered synthesis of spiro[indoline-3,4′-quinoline] via oxidative coupling of indole with enaminone and malononitrile
| dc.contributor.author | Maury S.K.; Kushwaha A.K.; Kamal A.; Singh H.K.; Singh S. | |
| dc.date.accessioned | 2025-05-23T11:17:54Z | |
| dc.description.abstract | In the most recent research, a straightforward, effective, and environmentally friendly method for producing spiro[indoline-3,4′-quinoline] was developed in ethanol using a photocatalyst eosin y and a 22 W LED lamp. This method involves the oxidative coupling of indole with enaminone and malononitrile. This method's key features include the absence of metals, low cost, environmental friendliness, greenness, non-toxicity, ease of handling, and use of renewable energy like visible light. This method exhibits a wide substrate scope for indole and active methylene compounds, including different enaminones. For the first time, spiro compounds were produced using visible light-mediated metal-free multicomponent synthesis under benign reaction conditions. © 2022 | |
| dc.identifier.doi | https://doi.org/10.1016/j.molstruc.2022.134452 | |
| dc.identifier.uri | http://172.23.0.11:4000/handle/123456789/7924 | |
| dc.relation.ispartofseries | Journal of Molecular Structure | |
| dc.title | Visible light triggered synthesis of spiro[indoline-3,4′-quinoline] via oxidative coupling of indole with enaminone and malononitrile |