5 research outputs found

    Homogeneous and Stereoselective Copper(II)-Catalyzed Monohydration of Methylenemalononitriles to 2‑Cyanoacrylamides

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    A facile and efficient route for the homogeneous and highly stereoselective monohydration of substituted methylenemalononitriles to (<i>E</i>)-2-cyanoacrylamides catalyzed by copper­(II) acetate monohydrate in acetic acid containing 2% water is described, and a mechanism is proposed. The protocol has proved to be suitable for the monohydration of dicyanobenzenes and 2-substituted malononitriles

    POCl<sub>3</sub>‑Mediated Reaction of 1‑Acyl-1-carbamoyl Oximes: A New Entry to Cyanoformamides

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    A facile and efficient one-pot synthesis of cyanoformamides was developed from readily available 1-acyl-1-carbamoyl oximes mediated by phosphoryl­trichloride (POCl<sub>3</sub>) under mild conditions in good to high yields

    Hydrogen Bond-Assisted 6π-Azaelectrocyclization of Penta-2,4-dienamides: Synthesis of Dihydropyridin-2(3<i>H</i>)‑ones

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    A facile and efficient synthesis of substituted dihydropyridin-2­(3<i>H</i>)-ones is developed from penta-2,4-dienamides, in which an intramolecular C–N bond was formed through thermal 6π-azaelectrocyclization. The intramolecular hydrogen bonding-assisted cyclization reaction opens access to a variety of dihydropyridin-2­(3<i>H</i>)-ones

    Homogeneous and Stereoselective Copper(II)-Catalyzed Monohydration of Methylenemalononitriles to 2‑Cyanoacrylamides

    No full text
    A facile and efficient route for the homogeneous and highly stereoselective monohydration of substituted methylenemalononitriles to (<i>E</i>)-2-cyanoacrylamides catalyzed by copper­(II) acetate monohydrate in acetic acid containing 2% water is described, and a mechanism is proposed. The protocol has proved to be suitable for the monohydration of dicyanobenzenes and 2-substituted malononitriles

    Homogeneous and Stereoselective Copper(II)-Catalyzed Monohydration of Methylenemalononitriles to 2‑Cyanoacrylamides

    No full text
    A facile and efficient route for the homogeneous and highly stereoselective monohydration of substituted methylenemalononitriles to (<i>E</i>)-2-cyanoacrylamides catalyzed by copper­(II) acetate monohydrate in acetic acid containing 2% water is described, and a mechanism is proposed. The protocol has proved to be suitable for the monohydration of dicyanobenzenes and 2-substituted malononitriles
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