Jump to main content
Jump to site search

Issue 2, 2016
Previous Article Next Article

Ferric perchlorate-mediated one-step reaction of [60]fullerene with primary amides for the synthesis of fullerooxazoles

Author affiliations

Abstract

The facile one-step reaction of [60]fullerene with primary amides promoted by cheap and easily available ferric perchlorate afforded a series of interesting fullerooxazole derivatives. The reaction was tolerant of a large variety of primary amides containing aryl, alkyl, and cinnamyl groups. A possible reaction mechanism for product formation was proposed.

Graphical abstract: Ferric perchlorate-mediated one-step reaction of [60]fullerene with primary amides for the synthesis of fullerooxazoles

Back to tab navigation

Supplementary files

Publication details

The article was received on 17 Sep 2015, accepted on 24 Nov 2015 and first published on 30 Nov 2015


Article type: Paper
DOI: 10.1039/C5NJ02503F
Author version
available:
Download author version (PDF)
New J. Chem., 2016,40, 1626-1632

  •   Request permissions

    Ferric perchlorate-mediated one-step reaction of [60]fullerene with primary amides for the synthesis of fullerooxazoles

    X. Zhang, F. Li, J. Shi, J. Wu and L. Liu, New J. Chem., 2016, 40, 1626
    DOI: 10.1039/C5NJ02503F

Search articles by author

Spotlight

Advertisements