Heterocyclization of fullerene with trifluoromethanesulfonamide

Capa

Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Somente assinantes

Resumo

The reaction of fullerene with trifluoromethanesulfonamide (triflamide), N , N -dichlorotriflamide and N -trifluoromethylsulfonyl(phenyl)iodinane in the presence of N -iodosuccinimide was studied. A single product of the aza[60]fulleroid structure was isolated.

Sobre autores

V. Astakhova

Irkutsk Institute of Chemistry A. E. Favorsky Siberian Branch of the Russian Academy of Sciences

Email: astakhova_vera@irioch.irk.ru

S. Zinchenko

Irkutsk Institute of Chemistry A. E. Favorsky Siberian Branch of the Russian Academy of Sciences

M. Moskalik

Irkutsk Institute of Chemistry A. E. Favorsky Siberian Branch of the Russian Academy of Sciences

Bibliografia

  1. Nagamachi T., Takeda Y., Nakayama K., Minakata S. Chem. Eur. J. 2012, 17, 12035-12045. doi: 10.1002/chem.201201680
  2. Miao C.-B., Lu X.-W., Wu P., Li J., Ren W.-L., Xing M.-L., Sun X.-Q., Yang H.-T. J. Org. Chem. 2013, 78, 12257-12262. doi: 10.1021/jo402079m
  3. Wu R., Lu X., Zhang Y., Zhang J., Xiong W., Zhu S. Tetrahedron. 2008, 64, 10694-10698. doi: 10.1016/j.tet.2008.09.016
  4. Tsuruoka R., Nagamachi T., Murakami Y., Komatsu M., Minakata S. J. Org. Chem. 2009, 74, 1691-1697. doi: 10.1021/jo8025737
  5. Yang H.-T., Lu X.-W., Xing M.-L., Sun X.-Q., Miao C.-B. Org. Lett. 2014, 16, 5882-5885. doi: 10.1021/ol5028305
  6. Sun Y., Qian C., Emge T.J., Li Y., Kopcha W.P., Wang L., Zhang J. Org. Lett. 2022, 24, 6417-6422. doi: 10.1021/acs.orglett.2c02494
  7. Yang H.-T., Ren W.-L., Dong C.-P., Yang Y., Sun X.-Q., Miao C.-B. Tetrahedron Lett. 2013, 54, 6799-6803. doi: 10.1016/j.tetlet.2013.09.002
  8. Yang H.-T., Liang X.-C., Wang Y.-H., Yang Y., Sun X.-Q., Miao C.-B. Org. Lett. 2013, 15, 4650-4653. doi: 10.1021/ol401909z
  9. Takeda Y., Enokijima S., Nagamachi T., Nakayama K., Minakata S. Asian J. Org. Chem. 2013, 2, 91-97. doi: 10.1002/ajoc.201200114
  10. Sunagawa S., Morisaki F., Baba T., Tsubouchi A., Yoshimura A., Miyamoto K., Uchiyama M., Saito A. Org. Lett. 2022, 24, 5230-5234. doi: 10.1021/acs.orglett.2c02264

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML
Baixar

Declaração de direitos autorais © Russian Academy of Sciences, 2023