2022
DOI: 10.1007/s11164-021-04637-x
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Design and characterization of [(Et)3 N-H]FeCl4 as a nanomagnetic ionic liquid catalyst for the synthesis of xanthene derivatives under solvent-free conditions

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Cited by 6 publications
(3 citation statements)
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“…densation of substituted benzaldehyde (47) and -naphthol (81; Scheme 22) under neat conditions. 76 The present catalyst was also explored for the synthesis of 3,4,6,7-tetrahydro-3,3,6,6-tetramethyl-9-aryl-2H-xanthene-1,8(5H,9H)diones (84) from 47 and dimedone (83) in 86-98% of yields. The ionic-liquid-based nanomagnetic catalysts were synthesised from triethyl amine with conc.…”
Section: Account Synlettmentioning
confidence: 99%
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“…densation of substituted benzaldehyde (47) and -naphthol (81; Scheme 22) under neat conditions. 76 The present catalyst was also explored for the synthesis of 3,4,6,7-tetrahydro-3,3,6,6-tetramethyl-9-aryl-2H-xanthene-1,8(5H,9H)diones (84) from 47 and dimedone (83) in 86-98% of yields. The ionic-liquid-based nanomagnetic catalysts were synthesised from triethyl amine with conc.…”
Section: Account Synlettmentioning
confidence: 99%
“…Ezabadi and Salami reported the triethyl ammonium ferric chloride catalysed synthesis of 14‑aryl‑14 H ‑dibenzo[ a , j ]xanthenes ( 82 ) via Knoevenagel–Michael cyclocondensation of substituted benzaldehyde ( 47 ) and β-naphthol ( 81 ; Scheme 22 ) under neat conditions. 76 The present catalyst was also explored for the synthesis of 3,4,6,7‑tetrahydro‑3,3,6,6‑tetramethyl‑9‑aryl‑2 H ‑xanthene‑1,8(5 H ,9 H )diones ( 84 ) from 47 and dimedone ( 83 ) in 86–98% of yields. The ionic-liquid-based nanomagnetic catalysts were synthesised from triethyl amine with conc.…”
Section: Aza- and Oxa-heterocycle Synthesis Catalysed By Mnpsmentioning
confidence: 99%
“…Ezabadi and Salami prepared a novel nanomagnetic ionic liquid [(Et) 3 NH]FeCl 4 by treating triethylamine with hydrochloric acid followed by the addition of ferric chloride hexahydrate, and used it to catalyze the synthesis of xanthene derivatives 3 and 5 (Scheme 1 ) under solvent-free conditions via Knoevenagel condensation of carbaldehydes 1 with β-naphthol ( 2 ) and dimedone ( 4 ). 48 The catalysts were assessed using FT-IR, Raman spectrometry, UV/visible spectrophotometry, TGA, FE-SEM, XRD, NMR, MS and VSM. Using an external magnet, the catalyst could be recovered and successfully reused for up to 5 cycles.…”
Section: Construction Of Heterocycles Catalyzed By Ionic Liquidsmentioning
confidence: 99%