Aziridino[2′,3′ : 1,2][60]fullerene
- 1 January 1995
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 8,p. 885-886
- https://doi.org/10.1039/c39950000885
Abstract
Thermal elimination of isobutene and CO2 from N-tert-butoxycarbonylaziridino[2′,3′ : 1,2][60]fullerene 4 provides a clean and efficient route to aziridino[2′,3′ : 1,2][60]fullerene 1, an isolable and stable solid.Keywords
This publication has 6 references indexed in Scilit:
- Chemical transformations on the surface of [60]fullerene: Synthesis of [60]fullereno[1′,2′:4,5]oxazolidin-2-oneTetrahedron Letters, 1994
- Bis-functionalisation of C60via thermal rearrangement of an isolable fulleroaziridine bearing a ‘solubilising’ supermesityl ester moietyJournal of the Chemical Society, Chemical Communications, 1994
- 1,2-Methanobuckminsterfullerene (C61H2), the parent fullerene cyclopropane: synthesis and structureJournal of the American Chemical Society, 1993
- Reaction of C60 with Dimethyldioxirane—Formation of an Epoxide and a 1,3‐Dioxolane DerivativeAngewandte Chemie International Edition in English, 1992
- Synthesis and characterization of C60O, the first fullerene epoxideJournal of the American Chemical Society, 1992
- Generation of carbethoxynitrene by .alpha. elimination and its reactions with olefins under two-phase conditionsThe Journal of Organic Chemistry, 1978