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
No coin nor oath required. For personal study only.
✦ 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-
📜 SIMILAR VOLUMES
**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,