A Facile and Green Synthesis of 2,4,6-Triarylpyridine Derivatives Using the Modified Mesoporous Organic Polymer Based on Calix [4]Resorcinarene: As an Efficient and Reusable Heterogeneous Acidic Catalyst


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Abstract

The work describes an efficient one-pot synthesis of 2,4,6-trisubstituted pyridine derivatives through a three-component catalytic reaction. The procedure involves mesoporous organic polymer based on calix[4]resorcinarene in and functionalized by N-propyl sulfamic acids a solid acid catalyst. Excellent yields, short reaction times, catalyst reusability, and easy reaction handling under solvent-free and mild acidic conditions are the most important advantages of the present protocol. The acidic catalyst was characterized by a number of spectroscopic methods such as Fourier-transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy and elemental CHNS analysis.

About the authors

A. Mouradzadegun

Department of Chemistry, Faculty of Science, Shahid Chamran University of Ahvaz; Center of Excellence in Electrochemistry, School of Chemistry, College of Science, University of Tehran

Author for correspondence.
Email: arash_m@scu.ac.ir
Iran, Islamic Republic of, Ahvaz; Tehran

M. A. Mostafavi

Department of Chemistry, Faculty of Science, Shahid Chamran University of Ahvaz

Author for correspondence.
Email: mostafavi.mahsa1366@yahoo.com
Iran, Islamic Republic of, Ahvaz

M. R. Ganjali

Center of Excellence in Electrochemistry, School of Chemistry, College of Science, University of Tehran; Biosensor Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute,
Tehran University of Medical Sciences

Author for correspondence.
Email: ganjali@khayam.ut.ac.ir
Iran, Islamic Republic of, Tehran; Tehran

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