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Cycloaddition of cage and polycyclic diazo compounds to C60 fullerene catalyzed by Pd(acac)2-2PPh3-4Et3Al
Authors:U. M. Dzhemilev  A. R. Tuktarov  V. V. Korolev  L. M. Khalilov
Affiliation:1.Institute of Petroleum Chemistry and Catalysis,Russian Academy of Sciences,Ufa, Bashkortostan,Russia
Abstract:Spirohomofullerenes were synthesized by cycloaddition of cage and polycyclic diazoalkanes generated in situ by oxidation of hydrazones of camphor, 2-adamantanone, and cholestane-3-one to C60 fullerene in the presence of the Pd(acac)2-2PPh3-4Et3Al three-component catalyst. It was found that the spiro-homofullerenes obtained from hydrazones of 2-adamantanone and cholestane-3-one and C60 fullerene do not undergo thermal isomerization to the corresponding spiro-methanofullerenes.
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