Aziridination of C60 with simple amides and catalytic rearrangement of the aziridinofullerenes to azafulleroids

R Tsuruoka, T Nagamachi, Y Murakami…

文献索引：Tsuruoka, Ryoji; Nagamachi, Toshiki; Murakami, Yuta; Komatsu, Mitsuo; Minakata, Satoshi Journal of Organic Chemistry, 2009 , vol. 74, # 4 p. 1691 - 1697

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被引用次数: 38

摘要

The selective formation of aziridinofullerene and azafulleroid, which are isomers of the fullerene derivatives-introduced N1 unit, is achieved. The ionic aziridination is a very convenient and risk-free procedure compared with the conventional method with azides as nitrogen sources, and gives aziridinofullerenes from various readily available amides (carbamates, ureas, carboxamides, and phosphamides). For example, benzyl carbamate ...