Issue 34, 2014

Magnetically recoverable and reusable CuFe2O4 nanoparticle-catalyzed synthesis of benzoxazoles, benzothiazoles and benzimidazoles using dioxygen as oxidant

Abstract

A green and efficient strategy for the synthesis of benzoxazoles, benzothiazoles and benzimidazoles has been developed by using inexpensive, readily available, dioxygen-stable and recyclable CuFe2O4 as the nanocatalyst, and o-substituted aminobenzene and various aldehydes as the starting materials. The CuFe2O4 nanoparticles are dioxygen insensitive and easily recoverable with an external magnet from the reaction medium. The catalyst can be reused ten times without significant loss of catalytic activity.

Graphical abstract: Magnetically recoverable and reusable CuFe2O4 nanoparticle-catalyzed synthesis of benzoxazoles, benzothiazoles and benzimidazoles using dioxygen as oxidant

Supplementary files

Article information

Article type
Paper
Submitted
22 Jan 2014
Accepted
01 Apr 2014
First published
03 Apr 2014

RSC Adv., 2014,4, 17832-17839

Author version available

Magnetically recoverable and reusable CuFe2O4 nanoparticle-catalyzed synthesis of benzoxazoles, benzothiazoles and benzimidazoles using dioxygen as oxidant

D. Yang, X. Zhu, W. Wei, N. Sun, L. Yuan, M. Jiang, J. You and H. Wang, RSC Adv., 2014, 4, 17832 DOI: 10.1039/C4RA00559G

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