An efficient functionalization of [60]fullerene. Diels-Alder reaction using 1,3-butadienes substituted with electron-withdrawing and electron-donating (silyloxy) groups-Reference-Cited by-同舟云学术

An efficient functionalization of [60]fullerene. Diels-Alder reaction using 1,3-butadienes substituted with electron-withdrawing and electron-donating (silyloxy) groups

Published:1996-04 Issue:14 Volume:52 Page:4983-4994
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ohno Masatomi,Azuma Toshihiro,Kojima Satoshi,Shirakawa Yuri,Eguchi Shoji

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference50 articles.

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2. Energetic preference in 5,6 and 6,6 ring junction adducts of C60: fulleroids and methanofullerenes

3. Aziridino[2′,3′ : 1,6][60]fullerene: isolation of the first closed [5,6]-bridged fullerene adduct

4. Cycloaddition Reactions of Fullerenes

5. The Chemistry of the Fullerenes;Hirsch,1994

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