2015
DOI: 10.1039/c4ra13045f
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Water mediated reactions: TiO2and ZnO nanoparticle catalyzed multi component domino reaction in the synthesis of tetrahydroacridinediones, acridindiones, xanthenones and xanthenes

Abstract: Tetrahydroacridine-1,8-(2H,5H,9H,10H)-diones 4 from 1,3-cyclohexanedione and/or dimedone 1,2-chloro-3-formylquinoline 2 and anilines 3 in water at 90 °C were obtained by domino reaction approach.

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Cited by 20 publications
(11 citation statements)
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“…[Scheme 12, Method 2]. Further, Pugazhenthia et al [96] . discovered ZnO and TiO 2 nano‐catalyzed synthesis of acridinediones using substituted 2‐chloro‐3‐formylquinoline/arylaldehydes, dimedone, RNH 2 /NH 4 OAc under conventional heating and MW irradiation.…”
Section: Synthesis Of Acridine‐18‐dione Derivativesmentioning
confidence: 99%
See 1 more Smart Citation
“…[Scheme 12, Method 2]. Further, Pugazhenthia et al [96] . discovered ZnO and TiO 2 nano‐catalyzed synthesis of acridinediones using substituted 2‐chloro‐3‐formylquinoline/arylaldehydes, dimedone, RNH 2 /NH 4 OAc under conventional heating and MW irradiation.…”
Section: Synthesis Of Acridine‐18‐dione Derivativesmentioning
confidence: 99%
“…After that, an adept, facile solvent-free, nanocrystalline TiO 2 catalyzed one pot MCR of 5,5dimethyl-1,3-cyclohexanedione and NH 4 OAc with substituted benzaldehydes to produce 1,8-dioxodecahydroacridines in moderate to excellent yields at 80°C was presented by Eidi et al [95] [Scheme 12, Method 2]. Further, Pugazhenthia et al [96] discovered ZnO and TiO 2 nano-catalyzed synthesis of acridine-diones using substituted 2-chloro-3-formylquinoline/arylaldehydes, dimedone, RNH 2 /NH 4 OAc under conventional heating and MW irradiation. Here, a range of products was synthesized in clean, safe and eco-friendly environment with high yields and recyclable catalyst [Scheme 12, Method 3,4].…”
Section: Nano-catalyzed Synthesismentioning
confidence: 99%
“…Nano‐Zinc oxide‐catalysed synthesis of xanthenones, xanthenediones and acridinones was developed by Khan et al . The cascade reaction of cyclohexane‐1,3‐dione, β ‐naphthol and arylaldehydes was carried out using 5 mol % ZnO in aqueous medium under microwave irradiation ( Scheme ) .…”
Section: Heterocyclic Compoundsmentioning
confidence: 99%
“…We considered the bondingi nformation of zinc salicylate/stearate to explain the bondingb etween f-CNFs and the zinc precursor.O wing to the oxidation treatment, the ÀCH 3 , ÀCH 2 , ÀCH, and ÀCOOH groups are attached to the surfaceo ft he nanofibers, as discussed in the FTIR and XPS analyses. (2)], as in the following processes: [57] Most of the zinc precursorsa re converted into zinc hydroxides [Eq.…”
Section: Mechanismmentioning
confidence: 99%