2013
DOI: 10.1007/s11164-013-1423-6
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Preparation of 2-amino-3-cyano-4-aryl-5,10-dioxo-5,10-dihydro-4H-benzo[g]chromene and hydroxyl naphthalene-1,4-dione derivatives

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Cited by 28 publications
(15 citation statements)
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“…These nanocatalysts have small size and large external surface areas that allow great accessibility of substrates to the surface‐bound active catalytic sites . Also, their applications are increased due to their superior characteristics such as easily removable from the reaction mixture using an external magnet and reuse for several times without significantly reducing in its catalytic activity …”
Section: Introductionmentioning
confidence: 99%
“…These nanocatalysts have small size and large external surface areas that allow great accessibility of substrates to the surface‐bound active catalytic sites . Also, their applications are increased due to their superior characteristics such as easily removable from the reaction mixture using an external magnet and reuse for several times without significantly reducing in its catalytic activity …”
Section: Introductionmentioning
confidence: 99%
“…The use of heterogeneous catalysts has been widely studied. These catalysts are easily removable from the reaction media by simple filtration after completion of the reaction and in many cases, they are reusable . Magnetic core‐shell nanostructures were forecast as magnetic strong catalysts in organic reactions.…”
Section: Introductionmentioning
confidence: 99%
“…The existence of many hydroxyl groups on the γ‐Fe 2 O 3 MNPs surface leads to a reaction with alkoxysilane reagents such as tetraethyl orthosilicate (TEOS) to form Si‐O bonds and provide reaction sites for further functionalization of γ‐Fe 2 O 3 /SiO 2 MSNPs . For the modification and functionalization of the surface of γ‐Fe 2 O 3 /SiO 2 MSNPs, the (3‐aminopropyl)triethoxysilane (APTES) and some silane reagents as potential candidates were used …”
Section: Introductionmentioning
confidence: 99%
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