2 research outputs found

    Heteropoly acid supported on activated natural clay-catalyzed synthesis of 3,4-dihydropyrimidinones/thiones through Biginelli reaction under solvent-free conditions

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    <p>Dihydropyrimidinones/thiones (DHPM’s) have been prepared by one-pot condensation of methyl acetoacetate, aldehydes, urea/thiourea in the presence of heteropoly-11-tungsto-1-vanadophosphoric acid, H<sub>4</sub>[PVW<sub>11</sub>O<sub>40</sub>] · 32H<sub>2</sub>O, (HPV) supported on activated natural clay (HPVAC) under solvent-free reaction condition have been proposed. The DHPM derivatives were identified through elemental analysis and melting point measurements and characterized by FT-IR, <sup>1</sup>H-NMR, <sup>13</sup>C-NMR spectroscopic methods.</p

    One-pot three-component synthesis of bis(indolyl)methanes under solvent-free condition using heteropoly-11-tungsto-1-vanadophosphoric acid supported on natural clay as catalyst

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    <p>One-pot three-component condensation reaction of two moles of indole and one mole of aromatic aldehyde for the synthesis of bis(indolyl)methanes in the presence of new catalytic material, heteropoly-11-tungsto-1-vanadophosphoric acid, H<sub>4</sub>[PV<sup>V</sup>W<sub>11</sub>O<sub>40</sub>] (HPV) supported on activated natural clay under solvent-free reaction condition has been proposed. The catalysts were prepared by incipient wetness impregnation method. The physicochemical characterizations of the HPV (20%) supported on natural clay (HPVAC-20) have also been discussed. Solvent-free heterogeneous reaction condition, simple workup procedure, short reaction time, high yield of products, and reusability of the catalyst are the advantages of the protocol.</p
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