F
Fariborz Mansouri
Researcher at Institute for Advanced Studies in Basic Sciences
Publications - 17
Citations - 709
Fariborz Mansouri is an academic researcher from Institute for Advanced Studies in Basic Sciences. The author has contributed to research in topics: Catalysis & Ionic liquid. The author has an hindex of 10, co-authored 16 publications receiving 593 citations. Previous affiliations of Fariborz Mansouri include Tarbiat Modares University & Malek-Ashtar University of Technology.
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Recent Applications of Magnetically Recoverable Nanocatalysts in CC and CX Coupling Reactions
TL;DR: In this article, the main synthetic steps required to develop both precious and nonprecious metal-catalyzed C and X coupling reactions by using magnetically separable catalysts are identified.
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A highly water-dispersible/magnetically separable palladium catalyst based on a Fe3O4@SiO2 anchored TEG-imidazolium ionic liquid for the Suzuki–Miyaura coupling reaction in water
TL;DR: In this article, an ionic liquid functionalized magnetic nanoparticle (IL-Pd) was prepared by anchoring an IMI liquid bearing triethylene glycol moieties on the surface of silica-coated iron oxide nanoparticles, which proved to be an effective host for the immobilization of a Pd catalyst through a subsequent simple ion-exchange process giving a highly water dispersible, active and yet magnetically recoverable Pd catalyzer.
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Ionic Liquids in Asymmetric Synthesis: An Overall View from Reaction Media to Supported Ionic Liquid Catalysis
TL;DR: A review of the use of ionic liquids in asymmetric transformations can be found in this article, where the authors survey ionic liquid reaction media for asymmetric reactions, including ionic-liquid-tagged chiral catalysts for use in synthesis.
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Synthesis and characterization of magnetic copper ferrite nanoparticles and their catalytic performance in one-pot odorless carbon-sulfur bond formation reactions
TL;DR: In this paper, a catalytic application of copper ferrite nanoparticles (CuFe 2 O 4 ) for one-pot odorless production of aryl alkyl thioethers using thiourea and bromides in wet polyethylene glycol as a green solvent was introduced.
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A Highly Water‐Dispersible/Magnetically Separable Palladium Catalyst: Selective Transfer Hydrogenation or Direct Reductive N‐Formylation of Nitroarenes in Water
TL;DR: The palladium catalyst demonstrated outstanding performance in aqueous-phase transfer hydrogenation of various nitroarenes in a highly chemo- and regioselective manner by using HCOONH4 as a low-cost, green, and easily available hydrogen donor.