Facile synthesis of arylated heterofullerenes ArC59N

Nuber B, Hirsch A (1998)


Publication Type: Journal article, Original article

Publication year: 1998

Journal

Original Authors: Nuber B., Hirsch A.

Publisher: Royal Society of Chemistry

Pages Range: 405-406

Journal Issue: 3

URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-0002769522&origin=inward

Abstract

The thermal treatment of the heterofullerene dimer (CN) with anisole, toluene and 1-chloronaphthalene in the presence of toluene-p-sulfonic acid and air leads to the formation monoarylated azafullerenes ArCN in very good yields.

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How to cite

APA:

Nuber, B., & Hirsch, A. (1998). Facile synthesis of arylated heterofullerenes ArC59N. Chemical Communications, 3, 405-406.

MLA:

Nuber, Berthold, and Andreas Hirsch. "Facile synthesis of arylated heterofullerenes ArC59N." Chemical Communications 3 (1998): 405-406.

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