2012
DOI: 10.5155/eurjchem.3.3.298-304.540
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Recyclable and reusable nano-CuFe2O4 catalyzed C-O cross-coupling

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Cited by 21 publications
(10 citation statements)
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“…However, unsubstituted bromobenzene resulted in a poor yield of the desired product and iodobenzene failed to participate in this reaction. 35 The comparison of the catalytic activity of 36 Very recently it is found that the use of cheaper and more readily available K 2 CO 3 as a base instead of Cs 2 CO 3 in this protocol produced similar yields of products. 37 2.5.…”
Section: Cui Nanoparticlesmentioning
confidence: 95%
“…However, unsubstituted bromobenzene resulted in a poor yield of the desired product and iodobenzene failed to participate in this reaction. 35 The comparison of the catalytic activity of 36 Very recently it is found that the use of cheaper and more readily available K 2 CO 3 as a base instead of Cs 2 CO 3 in this protocol produced similar yields of products. 37 2.5.…”
Section: Cui Nanoparticlesmentioning
confidence: 95%
“…If the catalyst is washed with distilled water and EtOAc, it can be reused six times with little decrease in its activity. Similarly, in 2012 Pallapothula and co‐workers reported the successful CuFe 2 O 4 ‐catalyzed CO cross‐coupling of phenols with aryl halides under ligand‐free conditions by using KOH as the base in DMSO at 120 °C 175. The CuFe 2 O 4 nanoparticles show better activity than other metal oxide nanoparticles such as Sb 2 O 3 , Y 2 O 3 , YFe 2 O 4 , Bi 2 O 3 , Co 3 O 4 , and SnO 2 in the CO cross‐coupling of aryl halides with phenol under identical reaction conditions.…”
Section: Cx Bond‐forming Reactionsmentioning
confidence: 98%
“…A ligand-free procedure for the coupling of oxygen nucleophiles with a wide range of aryl halides/alkyl halides (Scheme 13) has been developed by Pallapothulaet al [84] Here,reusable nano-CuFe 2 O 4 (6 mol%) catalyst was employed with the base KOHat120 °Cfor 20 h. Aryl halides withelectron-withdrawing groups at para-position displayed better reactivity compared to those with electron-donating groups. This catalytic system can be applied for aryl bromides also but with reduced efficiency than aryl iodides.…”
Section: Synthesis Of Diaryl Ethersmentioning
confidence: 99%