2018
DOI: 10.1016/j.jorganchem.2018.06.007
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Bisferrocene-containing ionic liquid supported on silica coated Fe 3 O 4 : A novel nanomagnetic catalyst for the synthesis of dihydropyrano[2,3- c ]coumarin derivatives

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Cited by 43 publications
(19 citation statements)
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“…We also synthesized a series of aromatic aldehydes (Scheme ), and applied them to synthesize new bis‐coumarin derivatives using condensation of these aldehydes and 4‐hydroxycoumarin catalyzed by Fe 3 O 4 @SiO 2 @Im‐bisethylFc [HC 2 O 4 ] nanocatalyst under optimized conditions (Table ) .…”
Section: Resultsmentioning
confidence: 99%
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“…We also synthesized a series of aromatic aldehydes (Scheme ), and applied them to synthesize new bis‐coumarin derivatives using condensation of these aldehydes and 4‐hydroxycoumarin catalyzed by Fe 3 O 4 @SiO 2 @Im‐bisethylFc [HC 2 O 4 ] nanocatalyst under optimized conditions (Table ) .…”
Section: Resultsmentioning
confidence: 99%
“…Then the solvent was removed by rotary evaporator and at the end the residue was purified by column chromatography. 5‐Chloro‐2,2‐bis (ethylferrocenyl) pentane was obtained in 65% yield as orange oil with relatively high viscosity …”
Section: Methodsmentioning
confidence: 99%
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“…2,3‐Dihydro‐5,6‐dimethoxy‐1‐indanone is a well‐known starting material in organic chemistry, but few reports are available on the study of optical properties of its derivatives . We previously mentioned some articles that focused on the investigation of electrochemical and optical properties of ferrocenyl derivatives . Because of the interesting properties of Fc as the optically and electrochemically active moiety and because of the prominent property of 2,3‐dihydro‐5,6‐dimethoxy‐1‐indanone in organic synthesis, here we report the preparation of a new ferrocenyl aldehyde bearing a 4‐chlorobutyl side chain.…”
Section: Introductionmentioning
confidence: 93%
“…The phenolic alcohol can also, if desired, be functionalized to introduce an aliphatic alcohol. Reza et al functionalized this phenolic position on vanillin by reacting it with 2-chloroethanol with catalytic potassium carbonate at reflux in DMSO for 6 h obtained 75% yield of 4-(2-hydroxyethoxy)-3-methoxybenzaldehyde [32]. Yang et al performed a similar reaction in dimethylformamide (DMF) at 100 • C for 5 h to obtain a yield only of 57% [33].…”
Section: Introductionmentioning
confidence: 99%