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    Bi(OTf)3-catalysed domino Friedel-Crafts alkylation of arenes with aldehydes: An upgraded method for efficient synthesis of triarylmethanes and anthracene derivatives

    , Article Tetrahedron ; Volume 72, Issue 11 , March , 2016 , Pages 1433–1439 ; 00404020 (ISSN) Mohammadiannejad Abbasabadi, K ; Mohammadpoor Baltork, I ; Tangestaninejad, S ; Moghadam, M ; Mirkhani, V ; Kia, R ; Sharif University of Technology
    Elsevier Ltd  2016
    Abstract
    A variety of novel triarylmethanes including bis-(dihexyloxyphenyl)arylmethanes and diveratrylmethanes were prepared by the domino Friedel-Crafts alkylation of arenes with aldehydes catalysed by Bi(OTf)3. The reaction of veratrole with aromatic dialdehydes afforded different results based on the molar ratio of reactants and the nature of aromatic dialdehydes. Bi(OTf)3/O2 is shown to be a highly efficient reagent system to promote the tandem three-step reaction of acylals with bis-(dihexyloxyphenyl)arylmethanes or diveratrylmethanes for the preparation of 9,10-disubstituted-2,3,6,7-tetraalkoxyanthracenes. The substrate scope, the simplicity of the reactions and work-up processes, besides a... 

    Bi(OTf)3-catalysed domino Friedel-Crafts alkylation of arenes with aldehydes: An upgraded method for efficient synthesis of triarylmethanes and anthracene derivatives

    , Article Tetrahedron ; Volume 72, Issue 11 , 2016 , Pages 1433-1439 ; 00404020 (ISSN) Mohammadiannejad Abbasabadi, K ; Mohammadpoor Baltork, I ; Tangestaninejad, S ; Moghadam, M ; Mirkhani, V ; Kia, R ; Sharif University of Technology
    Elsevier Ltd 
    Abstract
    A variety of novel triarylmethanes including bis-(dihexyloxyphenyl)arylmethanes and diveratrylmethanes were prepared by the domino Friedel-Crafts alkylation of arenes with aldehydes catalysed by Bi(OTf)3. The reaction of veratrole with aromatic dialdehydes afforded different results based on the molar ratio of reactants and the nature of aromatic dialdehydes. Bi(OTf)3/O2 is shown to be a highly efficient reagent system to promote the tandem three-step reaction of acylals with bis-(dihexyloxyphenyl)arylmethanes or diveratrylmethanes for the preparation of 9,10-disubstituted-2,3,6,7-tetraalkoxyanthracenes. The substrate scope, the simplicity of the reactions and work-up processes, besides a... 

    Synthesis of 1,4-disubstituted 1,2,3-triazoles from aromatic α-bromoketones, sodium azide and terminal acetylenes via Cu/Cu(OTf)2-catalyzed click reaction under microwave irradiation

    , Article Zeitschrift fur Naturforschung - Section C Journal of Biosciences ; Volume 68, Issue 4 , Apr , 2013 , Pages 391-396 ; 09395075 (ISSN) Fazeli, A ; Oskooie, H. A ; Beheshtiha, Y. S ; Heravi, M. M ; Matloubi Moghaddam, F ; Koushki Foroushani, B ; Sharif University of Technology
    2013
    Abstract
    Reaction of aromatic α-bromoketones, sodium azide and aromatic or aliphatic terminal acetylenes in the presence of Cu/Cu(OTf)2following the classical method (aqueous acetonitrile at room temperature) and under microwave irradiation (H2O at 85 °C) leads to 1,4-disubstituted 1,2,3-triazoles as the final products after simple filtration  

    New mononuclear manganese(II) complexes with 2,4,6-tris(2-pyridyl)-1,3,5- triazine (tptz) - Selective catalyst in UHP oxidation of sulfides

    , Article Polyhedron ; Volume 34, Issue 1 , February , 2012 , Pages 202-209 ; 02775387 (ISSN) Najafpour, M. M ; Hołyńska, M ; Shamkhali, A. N ; Amini, M ; Kazemi, S. H ; Zaynalpoor, S ; Mohamadi, R ; Bagherzadeh, M ; Lis, T ; Sharif University of Technology
    2012
    Abstract
    A new manganese complex of the formula [Mn(tptz)(OH 2) 3](CF 3SO 3) 2·EtOH, (1, where tptz = (2,4,6-tris(2-pyridyl)-1,3,5-triazine) is presented, exhibiting an excellent catalytic activity and selectivity in oxidation of various sulfides to the corresponding sulfoxides with UHP (urea hydrogen peroxide) as oxidant under air at room temperature. A modified preparation procedure produces another new manganese complex of the formula [Mn(tptz)(CH 3COO)(OH 2) 2](CF 3SO 3)·3H 2O (2). X-ray structures of both Mn(II) complexes, properties (elemental analysis, electrochemistry, EPR, IR, Raman, and UV-Vis spectra), as well as DFT studies results are reported  

    Gadolinium triflate immobilized on magnetic nanocomposites as recyclable Lewis acid catalyst for acetylation of phenols

    , Article Nanoscience and Nanotechnology Letters ; Vol. 6, issue. 4 , 2014 , p. 309-313 Rafiaei, S. M ; Kim, A ; Shokouhimehr, M ; Sharif University of Technology
    Abstract
    The acetylation of phenols with acetic anhydride proceeded in excellent yields when it was catalyzed by gadolinium triflate immobilized on magnetically recyclable nanocomposites. This heterogeneous catalyst provided high catalytic activity with low loading level (1 mol%), because the Lewis acid catalyst was grafted on the surface of the nanocomposites. The catalysts were also easily recovered from the reaction mixture using a magnet and reused for six consecutive cycles