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    Microwave-expedited synthesis of aromatic aldehydes and ketones from alkyl halides without solvent using wet montmorillonite K 10 supported iodic acid as oxidant

    , Article Acta Chimica Slovenica ; Volume 51, Issue 2 , 2004 , Pages 333-336 ; 13180207 (ISSN) Mahmoudi Hashemi, M ; Rahimi, A ; Ahmadibeni, Y ; Sharif University of Technology
    2004
    Abstract
    The efficient microwave-assisted synthesis of aldehydes and ketones over wet montmorillonite K 10 using HIO3 as oxidizing agent is described. This fast oxidation protocol is applicable to variety of alkyl halides  

    Versatile and large-scale synthesis of functional dithiocarbamates in water

    , Article Synthetic Communications ; Volume 41, Issue 1 , Dec , 2011 , Pages 94-99 ; 00397911 (ISSN) Azizi, N ; Aryanasab, F ; Tourkian, L ; Saidi, M. R ; Sharif University of Technology
    2011
    Abstract
    Structural diversity is possible in direct access to functional dithiocarbamates based on a highly efficient and simple one-pot reaction of CS2, amines, and alkyl halides in nearly quantitative yields in water  

    A novel one-pot synthesis of 2-alkylthio-1,3,4-oxadiazoles in water

    , Article Journal of the Iranian Chemical Society ; Volume 8, Issue 2 , June , 2011 , Pages 525-530 ; 1735207X (ISSN) Aryanasab, F ; Maleki, H ; Saidi, M. R ; Sharif University of Technology
    2011
    Abstract
    A facile and one-pot protocol for the synthesis of 2-alkylthio-1,3,4- oxadiazoles is reported. This green method relies on the reaction of acid hydrazides with CS2 and an alkyl halide. The reaction is carried out under mild and environmentally friendly procedure in water with high to excellent yields. Thirteen different valuable alkylthio-1,3,4-oxadiazoles are synthesized from cheap and easily available CS2 with this method. This is the first report for the synthesis of 1,3,4-oxadiazoles in water  

    A novel highly dispersive magnetic nanocatalyst in water : Glucose as an efficient and green ligand for the immobilization of copper(II) for the cycloaddition of alkynes to azides

    , Article RSC Advances ; Volume 6, Issue 83 , 2016 , Pages 80234-80243 ; 20462069 (ISSN) Matloubi Moghaddam, F ; Saberi, V ; Kalhor, S ; Ayati, S. E ; Sharif University of Technology
    Royal Society of Chemistry 
    Abstract
    A new heterogeneous and highly dispersive nanocatalyst in water was prepared by the immobilization of Cu2+ onto glucose on Fe3O4. The catalyst was fully characterized by FT-IR, TGA, CHN, SEM, EDX, and atomic absorption spectroscopy. The synthesized catalyst was used in the synthesis of different derivatives of 1,2,3-triazole via a one-pot three-component reaction of alkynes, alkyl halides, and sodium azide. To the best of our knowledge, this novel catalyst adheres to the principles of green chemistry. The nanocatalyst could be recycled and reused in several runs without significant loss of activity  

    Copper immobilized onto a triazole functionalized magnetic nanoparticle: A robust magnetically recoverable catalyst for "click" reactions

    , Article RSC Advances ; Volume 5, Issue 5 , 2015 , Pages 3894-3902 ; 20462069 (ISSN) Matloubi Moghaddam, F ; Ayati, S. E ; Sharif University of Technology
    Abstract
    A novel magnetic heterogeneous copper catalyst was synthesized by immobilization of copper ions onto triazole functionalized Fe3O4. The catalyst was fully characterized by FT-IR, TGA, CHN, SEM, TEM, EDX and atomic adsorption spectroscopy. The resulting catalyst was used in the synthesis of 1,2,3-triazoles via a one-pot three component reaction of alkynes, alkyl halides, sodium azides under green conditions. The catalyst was reused ten times and no significant loss of activity was observed