104 research outputs found

    In situ generated hypoiodous acid in an efficient and heterogeneous catalytic system for the homo-oxidative coupling of thiols

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    Supported hydrogen peroxide on polyvinylpolypyrrolidone (PVPH2O2), silica sulfuric acid (SiO2-OSO3H) and catalytic amounts of potassium iodide (KI) has been developed as a heterogeneous medium for the rapid oxidative coupling of thiols into symmetrical homodisulfides. This oxidizing system proceeds under extremely mild conditions and gives no other oxidized side products

    A magnetically-separable H3PW12O40@Fe3O4/EN-MIL-101 catalyst for the one-pot solventless synthesis of 2H-indazolo[2,1-b] phthalazine-triones

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    A magnetic inorganic-organic catalyst, PTA@Fe3O4/EN-MIL-101 (EN = ethylenediamine, PTA = phosphotungstic acid) was fabricated and characterized by XRD, HRTEM, FESEM, UV–vis, TGA-DTA, FT-IR, XPS and porosimetry. PTA retained the parent Keggin structure upon dispersion throughout the amine-functionalized chromium terephthalate metal-organic framework, over which magnetic Fe3O4 nanoparticles were previously introduced. The resulting composite heterogeneous solid acid was an active catalyst for the one-pot synthesis of diverse 2H-indazolo[2,1-b] phthalazine-triones in good → excellent yields under mild, solventless condition, and offers facile separation and excellent recyclability

    A new method for the oxidation of 1, 4-dihydropyridine derivatives by guanidinium nitrate in the presence of silica sulfuric acid under mild, heterogeneous and metal-free conditions

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    In this paper, a new and convenient method is introduced for the oxidation of a variety of Hantzsch 1, 4-dihydropyridine derivatives to their corresponding pyridine compounds using guanidinium nitrate and silica sulfuric acid. The reactions were carried out in dichloromethane at room temperature and the products were isolated at high to excellent yields

    A new method for the oxidation of 1, 4-dihydropyridine derivatives by guanidinium nitrate in the presence of silica sulfuric acid under mild, heterogeneous and metal-free conditions

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    AbstractIn this paper, a new and convenient method is introduced for the oxidation of a variety of Hantzsch 1, 4-dihydropyridine derivatives to their corresponding pyridine compounds using guanidinium nitrate and silica sulfuric acid. The reactions were carried out in dichloromethane at room temperature and the products were isolated at high to excellent yields
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