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Visible light triggered synthesis of spiro[indoline-3,4′-quinoline] via oxidative coupling of indole with enaminone and malononitrile

dc.contributor.authorMaury S.K.; Kushwaha A.K.; Kamal A.; Singh H.K.; Singh S.
dc.date.accessioned2025-05-23T11:17:54Z
dc.description.abstractIn 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.doihttps://doi.org/10.1016/j.molstruc.2022.134452
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/7924
dc.relation.ispartofseriesJournal of Molecular Structure
dc.titleVisible light triggered synthesis of spiro[indoline-3,4′-quinoline] via oxidative coupling of indole with enaminone and malononitrile

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