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Masoud Mokhtary - One of the best experts on this subject based on the ideXlab platform.

  • Application of PVPP-OXA as an efficient catalyst for the synthesis of mono and bulky 1,8-dioxooctahydroxanthenes
    2019
    Co-Authors: Reza Dezhanga, Masoud Mokhtary
    Abstract:

    An efficient method for the synthesis of mono and bulky 1,8-dioxooctahydroxanthenes was developed by the reaction of dimedone or 1,3-cyclohexadione and aldehydes or some bisaldehydes in the presence of Polyvinylpolypyrrolidone supported oxalic acid (PVPP-OXA) as a new polymeric catalyst in ethanol at room temperature. Polyvinylpolypyrrolidone supported oxalic acid was characterized by FT-IR, and TGA analysis. Clean methodologies, simple preparation of the catalyst, high yields, environment-friendly and reusable catalyst are some advantages of this work.

  • Polyvinylpolypyrrolidone supported chlorosulfonic acid: An efficient catalyst for the one-pot synthesis of hexahydroquinolines
    iranian journal of catalysis, 2016
    Co-Authors: Mahshid Yosefzadeh, Masoud Mokhtary
    Abstract:

    Polyvinylpolypyrrolidone supported chlorosulfonic acid ([PVPP-SO3H] + Cl - ) was synthesized and evaluated as a recoverable catalyst for the one-pot synthesis of hexahydroquinolines by reaction of arylaldehydes, dimedone (5,5-dimethylcyclohexane1,3-dione) or 1,3-cyclohexanedione, ethylacetoacetate and ammonium acetate in high to excellent yield in ethanol at 70 °C. The [PVPP-SO3H] + Cl - catalyst was characterized via Fourier transform infrared spectroscopy (FT-IR) and thermal gravimetric analysis (TGA). The acidity strength of the catalyst was determined by titration and found to be 12 mmol/g, which shows a high loading of H + per gram of the catalyst. Moreover, the catalyst could be recycled several times without significant loss of its catalytic activity. Clean methodologies, easy work-up procedure, high yield and simple preparation of the catalyst are some advantages of this work.

  • Polyvinylpolypyrrolidone-supported boron trifluoride: a mild and efficient catalyst for the synthesis of 1,8-dioxooctahydroxanthenes and 1,8-dioxodecahydroacridines
    Monatshefte Fur Chemie, 2014
    Co-Authors: Masoud Mokhtary, Seyed Abdollah Mirfarjood Langroudi
    Abstract:

    Polyvinylpolypyrrolidone-supported boron trifluoride has been studied for the synthesis of 1,8-dioxooctahydroxanthenes and 1,8-dioxodecahydroacridines. The reaction proceeded via condensation of: (1) aromatic aldehydes (1 eq.) and 5,5-dimethyl-1,3-cyclohexanedione (2 eq.) in acetonitrile at room temperature, (2) aromatic aldehydes (1 eq.), 5,5-dimethyl-1,3-cyclohexanedione (2 eq.), and aromatic amines (1 eq.) in acetonitrile at 80 °C in the presence of Polyvinylpolypyrrolidone-supported boron trifluoride. This procedure cleanly converted a variety of aryl aldehydes with different substituent groups at ortho, meta, or para positions to the corresponding products. Convenience and efficiency, an easy work-up procedure, high yield, and simple preparation of the catalyst are some advantages of this method. In addition, the Polyvinylpolypyrrolidone-supported boron trifluoride complex is a high loaded Lewis acid, which is stable, easy to handle, and retains effective activity after several months of storage.

  • Polyvinylpolypyrrolidone-supported boron trifluoride (PVPP-BF3): Mild and efficient catalyst for the synthesis of 14-aryl-14H-dibenzo [a,j] xanthenes and bis(naphthalen-2-yl-sulfane) derivatives
    Dyes and Pigments, 2013
    Co-Authors: Masoud Mokhtary, Sepideh Refahati
    Abstract:

    Abstract A convenient and an efficient method for the synthesis of 14-aryl-14 H -dibenzo [a,j] xanthenes and bis(naphthalen-2-yl-sulfane) derivatives is described. The reaction proceeded via condensation of aldehydes with 2-naphthol or 2-thionaphthol in the presence of Polyvinylpolypyrrolidone-supported boron trifluoride. These reactions were studied under different conditions. In terms of reaction time and yield, it was found that optimum results were obtained for the synthesis of 14-aryl-14 H -dibenzo [a,j] xanthenes under solvent free technique at 120 O C and for preparation of bis(naphthalen-2-yl-sulfane) derivatives in 1,2-dichloroethan under reflux conditions. Clean methodologies, easy workup procedure, high yield and simple preparation of the catalyst are some advantages of this work.

  • Polyvinylpolypyrrolidone-bound boron trifluoride (PVPP-BF3); a mild and efficient catalyst for synthesis of 4-metyl coumarins via the Pechmann reaction
    Comptes Rendus Chimie, 2012
    Co-Authors: Masoud Mokhtary, Faranak Najafizadeh
    Abstract:

    Abstract Polyvinylpolypyrrolidone-supported boron trifluoride has been studied for synthesis of 4-methyl coumarin by the Pechmann reaction. The reaction proceeded smoothly with hydroxyl phenols and ethyl acetoacetate in good yields in ethanol at reflux conditions. The Polyvinylpolypyrrolidone-boron trifluoride complex is a non-corrosive and stable solid catalyst elevated Lewis acid property.

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