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Can I read Diels–Alder reaction of [60]fullerene with cyclooctatetraene and electrophilic addition to the cycloadduct on EtoBox?

Diels–Alder reaction of [60]fullerene with cyclooctatetraene and electrophilic addition to the cycloadduct by Hiroshi Ishida; Kenichi Komori; Kenji Itoh*; Masatomi Ohno is a Chemistry article available to read on EtoBox.

What is Diels–Alder reaction of [60]fullerene with cyclooctatetraene and electrophilic addition to the cycloadduct about?

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 addition reactions in a manner somewhat different from the usual reactions.

Who reads Diels–Alder reaction of [60]fullerene with cyclooctatetraene and electrophilic addition to the cycloadduct?

It is typically read by researchers, students, and practitioners in Chemistry.

Author
Hiroshi Ishida; Kenichi Komori; Kenji Itoh*; Masatomi Ohno
Publisher
Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0040-4039)
Published
2000
Language
EN
Field
Chemistry (Physical Sciences)

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