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Aziridinofullerene: a versatile platform for functionalized fullerenes
Authors:Nambo Masakazu  Segawa Yasutomo  Itami Kenichiro
Affiliation:Department of Chemistry, Graduate School of Science, Nagoya University, Nagoya, Japan.
Abstract:An aziridine moiety on the fullerene core can serve as an acid-triggered reacting template for the controlled synthesis of a range of functionalized fullerenes that are otherwise difficult to synthesize in an efficient and selective manner. A copper-catalyzed aziridination of C(60) for the practical synthesis of aziridinofullerene 1 and acid-catalyzed reactions of 1 with mono- and bifunctional nucleophiles as well as alkynes are described. The rapid generation of structural diversity in a single chemical operation using the common platform 1 is notable.
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