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Selective Electrochemical Retro-Cycloaddition Reaction of Pyrrolidinofullerenes

✍ Scribed by Olena Lukoyanova; Claudia M. Cardona; Margarita Altable; Salvatore Filippone; Ángel Martín Domenech; Nazario Martín; Luis Echegoyen


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
156 KB
Volume
118
Category
Article
ISSN
0044-8249

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✦ Synopsis


Since the discovery of fullerenes, various methods for their functionalization have been developed and explored extensively. [1] Among the most widely employed derivatization reactions are Diels-Alder cycloadditions, [2] cyclopropanations, [3] and azomethine 1,3-dipolar cycloaddition reactions. [4] The cyclopropanation reaction, [3a] which forms a cyclopropano (methano) addend on the fullerene sphere, and the 1,3-


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Cover Picture: Retro-Cycloaddition React
✍ Nazario Martín; Margarita Altable; Salvatore Filippone; Angel Martín-Domenech; L 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 176 KB 👁 2 views

**Retro‐cycloaddition** of easily prepared pyrrolidinofullerenes affords quantitatively pristine fullerenes, and thus can be used as a new protection‐deprotection protocol in the chemistry of fullerenes, as shown in the cover picture. In their Communication on page 110 ff., N. Martín, L. Echegoyen,