NEW ROUTE FOR [60]FULLERENE FUNCTIONALIZATION IN [4+2]CYCLOADDITION REACTION USING INDENE

Authors
PUPLOVSKIS A KACENS J NEILANDS O
Citation
A. Puplovskis et al., NEW ROUTE FOR [60]FULLERENE FUNCTIONALIZATION IN [4+2]CYCLOADDITION REACTION USING INDENE, Tetrahedron letters, 38(2), 1997, pp. 285-288
Citations number
23
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
38
Issue
2
Year of publication
1997
Pages
285 - 288
Database
ISI
SICI code
0040-4039(1997)38:2<285:NRF[FI>2.0.ZU;2-V
Abstract
The Diels-Alder [4+2] cycloaddition of isoindene, generated in situ fr om indene, to [60]fullerene, yielded the new [60]fullerene derivative 1. The product was isolated by column chromatography and spectroscopic ally characterized. This method provides a new route to derivatives wh ere functional groups can be rigidly attached to the [60]fullerene cag e. Copyright (C) 1996 Elsevier Science Ltd