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Information Journal Paper

Title

Multi-component one-pot synthesis of tetrasubstituted pyrroles by silica molybdic acid under solvent-free conditions

Pages

  111-123

Abstract

 A variety of tetrasubstituted pyrroles were synthesized by a one-pot three-component reaction of α-hydroxyketones (benzoin derivatives), malononitrile, and ammonium acetate in good yields under solvent-free conditions. In these reactions silica molybdic acid (SMA) was used as efficient, reusable, green and useful catalyst. The prepared silica molybdic acid (SMA) was characterized by X-ray fluorescence (XRF), powdered X-ray diffraction (XRD), and FT-IR spectroscopy. The attractive advantages of this method are the short reaction times, high yields of the products and reusability of the catalyst. All of these advantages make it a useful strategy for the preparation of various pyrrole derivatives simply by different substrates.

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    APA: Copy

    Farahi, Mahnaz, KARAMI, BAHADOR, & Davoodi, Mahdiyeh. (2018). Multi-component one-pot synthesis of tetrasubstituted pyrroles by silica molybdic acid under solvent-free conditions. JOURNAL OF APPLIED CHEMISTRY, 13(48 ), 111-123. SID. https://sid.ir/paper/383405/en

    Vancouver: Copy

    Farahi Mahnaz, KARAMI BAHADOR, Davoodi Mahdiyeh. Multi-component one-pot synthesis of tetrasubstituted pyrroles by silica molybdic acid under solvent-free conditions. JOURNAL OF APPLIED CHEMISTRY[Internet]. 2018;13(48 ):111-123. Available from: https://sid.ir/paper/383405/en

    IEEE: Copy

    Mahnaz Farahi, BAHADOR KARAMI, and Mahdiyeh Davoodi, “Multi-component one-pot synthesis of tetrasubstituted pyrroles by silica molybdic acid under solvent-free conditions,” JOURNAL OF APPLIED CHEMISTRY, vol. 13, no. 48 , pp. 111–123, 2018, [Online]. Available: https://sid.ir/paper/383405/en

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