Jump to main content
Jump to site search

Issue 13, 2009
Previous Article Next Article

A facile access to [60]fullerene-fused δ-lactones: unexpected reaction pathway of benzenediazonium-2-carboxylates controlled by organic bases

Author affiliations

Abstract

The reaction of [60]fullerene with anthranilic acids and isoamyl nitrite in the presence of triethylamine unexpectedly afforded [60]fullerene-fused δ-lactones, which would be difficult to be prepared by other known methods; the organic base played a crucial role in the unusual reaction pathway.

Graphical abstract: A facile access to [60]fullerene-fused δ-lactones: unexpected reaction pathway of benzenediazonium-2-carboxylates controlled by organic bases

Back to tab navigation

Supplementary files

Publication details

The article was received on 14 Nov 2008, accepted on 08 Jan 2009 and first published on 04 Feb 2009


Article type: Communication
DOI: 10.1039/B820395D
Chem. Commun., 2009, 1769-1771

  •   Request permissions

    A facile access to [60]fullerene-fused δ-lactones: unexpected reaction pathway of benzenediazonium-2-carboxylates controlled by organic bases

    G. Wang and B. Zhu, Chem. Commun., 2009, 1769
    DOI: 10.1039/B820395D

Search articles by author

Spotlight

Advertisements