Issue 13, 2014

A simple, green, one-pot synthesis of magnetic-nanoparticle-supported proline without any source of supplemental linkers and application as a highly efficient base catalyst

Abstract

Fe3O4–proline MNPs were synthesized without any supplemental linkers, using an eco-friendly and effective procedure. It is readily loaded onto magnetic nanoparticles in a single step and is capable of promoting a range of synthetically useful reactions at ambient conditions. Functionalized chromene derivatives are synthesized via condensation and ring annulations of 2-hydroxynaphthalene-1,4-dione or 4-hydroxycoumarin, aryl aldehyde and malononitrile in the presence of a catalytic amount of Fe3O4–proline MNPs at room temperature in excellent yields.

Graphical abstract: A simple, green, one-pot synthesis of magnetic-nanoparticle-supported proline without any source of supplemental linkers and application as a highly efficient base catalyst

Article information

Article type
Communication
Submitted
05 Nov 2013
Accepted
15 Nov 2013
First published
18 Nov 2013

RSC Adv., 2014,4, 6508-6512

A simple, green, one-pot synthesis of magnetic-nanoparticle-supported proline without any source of supplemental linkers and application as a highly efficient base catalyst

K. Azizi and A. Heydari, RSC Adv., 2014, 4, 6508 DOI: 10.1039/C3RA46419A

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