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Diels-Alder reactions of the [60]fullerene functionalizing a carbon sphere with flexibly and with rigidly bound addends

✍ Scribed by Bernhard Kräutler; Josef Maynollo

Publisher
Elsevier Science
Year
1996
Tongue
French
Weight
472 KB
Volume
52
Category
Article
ISSN
0040-4020

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60]Fullerene reacted with cyclooctatetraene as a dienic partner in the Diels-Alder reaction to give the 1:1 cycloadduct in satisfactory yield (51%), which was attained by heating at relatively low temperature (110°C) and for an extended period (2 days). The cycloadduct underwent electrophilic additi

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