Title of article
Diels–Alder reaction of [60]fullerene with cyclooctatetraene and electrophilic addition to the cycloadduct
Author/Authors
Ishida، نويسنده , , Hiroshi and Komori، نويسنده , , Kenichi and Itoh*، نويسنده , , Kenji and Ohno *، نويسنده , , Masatomi، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
4
From page
9839
To page
9842
Abstract
[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.
Keywords
cyclooctatetraene , Diels–Alder reaction , electrophilic addition reaction , self-sensitized photooxygenation
Journal title
Tetrahedron Letters
Serial Year
2000
Journal title
Tetrahedron Letters
Record number
1640520
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