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Information Journal Paper

Title

ACIDIC BRONSTED IONIC LIQUIDS CATALYZED THE PREPARATION OF 2-AMINO-3-CYANOPYRIDINE DERIVATIVES UNDER AMBIENT AND SOLVENT-FREE CONDITIONS

Pages

  11-20

Abstract

 The ACIDIC IONIC LIQUIDS, 2-pyrrolidonium hydrogensulfate, N -methyl-2-pyrrolidonium hydrogensulfate, triphenyl (propyl-3-sulphonyl) phosphonium toluenesulfonate and (4-sulfobutyl) tris (4-sulfophenyl) phosphonium hydrogensulfate catalyzed one-pot four-component condensation between AROMATIC ALDEHYDES, substituted ACETOPHENONES, MALONONITRILE and AMMONIUM ACETATE to afford corresponding 2-amino-3-cyanopyridine derivatives. This synthetic method has the remarkable advantages such as mild reaction conditions and good isolated yields, short reaction time, and use of green catalysts.

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    • Cite

    APA: Copy

    Mollashahi, Ebrahim, & Bazgiri, Ali. (2018). ACIDIC BRONSTED IONIC LIQUIDS CATALYZED THE PREPARATION OF 2-AMINO-3-CYANOPYRIDINE DERIVATIVES UNDER AMBIENT AND SOLVENT-FREE CONDITIONS. JOURNAL OF APPLIED CHEMISTRY, 12(45), 11-20. SID. https://sid.ir/paper/693914/en

    Vancouver: Copy

    Mollashahi Ebrahim, Bazgiri Ali. ACIDIC BRONSTED IONIC LIQUIDS CATALYZED THE PREPARATION OF 2-AMINO-3-CYANOPYRIDINE DERIVATIVES UNDER AMBIENT AND SOLVENT-FREE CONDITIONS. JOURNAL OF APPLIED CHEMISTRY[Internet]. 2018;12(45):11-20. Available from: https://sid.ir/paper/693914/en

    IEEE: Copy

    Ebrahim Mollashahi, and Ali Bazgiri, “ACIDIC BRONSTED IONIC LIQUIDS CATALYZED THE PREPARATION OF 2-AMINO-3-CYANOPYRIDINE DERIVATIVES UNDER AMBIENT AND SOLVENT-FREE CONDITIONS,” JOURNAL OF APPLIED CHEMISTRY, vol. 12, no. 45, pp. 11–20, 2018, [Online]. Available: https://sid.ir/paper/693914/en

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