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Issue 13, 2009
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A facile access to [60]fullerene-fused δ-lactones: unexpected reaction pathway of benzenediazonium-2-carboxylates controlled by organic bases

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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

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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
Citation: Chem. Commun., 2009,0, 1769-1771

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    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, 0, 1769
    DOI: 10.1039/B820395D

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