Abstract
It has been shown that, depending on the structure, the products of dehydrochlorination of N-benzyltrifluoroacetimidoyl chlorides react with C60 under the action of triethylamine as a [3 + 2] cycloaddition (with the formation of fulleropyrrolines) or a [4 + 2] cycloaddition (with the formation of fulleropiperideines).
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
REFERENCES
M. V. Reinov, M. A. Yurovskaya, D. V. Davydov, and A. V. Streletskiy, Khim. Geterotsikl. Soedin., 223 (2004).
M. A. Yurovskaya and I. V. Trushkov, Izv. Russ. Akad. Nauk, Ser. Khim., 343 (2002).
M. A. Yurovskaya and A. A. Ovcharenko, Khim. Geterotsikl. Soedin., 291 (1998).
J. Averdung, E. Albrecht, J. Lauterwein, J. Mattay, H. Mohn, W. H. Muller, and H. U. ter Meer, Chem. Ber., 127, 787 (1994).
A. A. Ovcharenko, V. A. Chertkov, A. V. Karchava, and M. A. Yurovskaya, Tetrahedron Lett., 38, 6933 (1997).
P. P. Demenuk, M. V. Reinov, A. A. Ovcharenko, and M. A. Yurovskaya, Abstracts. 4 th Biennial Int. Workshop in Russia “Fullerenes and Atomic Clusters”, St-Petersburg (1999), P-188.
T. Brown, N. L. Clipston, N. Simjee, H. Luftmann, H. Hungerbuhler, and T. Drewello, Int. J. Mass Spectrom., 210, 249 (2001).
K. Tanaka, H. Daikaku, and K. Mitsuhashi, Chem. Lett., 1463 (1983).
K. Tanaka, H. Daikaku, and K. Mitsuhashi, Heterocycles, 21, 611 (1984).
A. V. Streletskiy, I. V. Kouvitchko, S. E. Esipov, and O. V. Boltalina, Rapid Commun. Mass Spectrom., 16, 99 (2002).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Reinov, M.V., Yurovskaya, M.A., Streletskiy, A.V. et al. Heterocyclic Derivatives of Fullerene C60. 2. Cycloaddition to Fullerene C60 of the Products of Dehydrochlorination of N-Benzyltrifluoroacetimidoyl Chlorides. Chemistry of Heterocyclic Compounds 40, 1150–1154 (2004). https://doi.org/10.1023/B:COHC.0000048287.59108.e2
Issue Date:
DOI: https://doi.org/10.1023/B:COHC.0000048287.59108.e2