Issue 8, 2004

Selective addition to [60]fullerene of two different radicals generated from Mn(iii)-based radical reaction

Abstract

Reaction of [60]fullerene in toluene with diethyl methylmalonate (3a), diethyl ethylmalonate (3b), diethyl bromomalonate (3c), triethyl methanetricarboxylate (3d) and ethyl cyanoacetate (3e) in the presence of manganese(III) acetate dihydrate afforded benzyl-substituted unsymmetrical 1,4-adducts 4a–4e. Dibenzylated 1,4-adduct 5 and methanofullerene 6 were also obtained in the case of 3d and 3e, respectively. A possible reaction mechanism for the formation of the 1,4-adducts 4a–4e is proposed.

Graphical abstract: Selective addition to [60]fullerene of two different radicals generated from Mn(iii)-based radical reaction

Article information

Article type
Paper
Submitted
05 Jan 2004
Accepted
27 Feb 2004
First published
18 Mar 2004

Org. Biomol. Chem., 2004,2, 1160-1163

Selective addition to [60]fullerene of two different radicals generated from Mn(III)-based radical reaction

G. Wang, T. Zhang, X. Cheng and F. Wang, Org. Biomol. Chem., 2004, 2, 1160 DOI: 10.1039/B317084E

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