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Photochemical cyclization of anils of polyfluoroaromatic ketones

  • Organic Chemistry
  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

The UV irradiation of the anils polyfluoroaromatic ketones in strongly acidic media leads to photochemical cyclization to phenanthridines. The insertion of substituents into the anil molecule lowers the phototransformation rate.

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Authors and Affiliations

  1. Novosibirsk Institute of Organic Chemistry, Siberian Branch of Academy of Sciences of the USSR, USSR

    N. I. Danilenko, T. V. Fomenko, I. K. Korobeinicheva, T. N. Gerasimova & E. P. Fokin

Authors
  1. N. I. Danilenko
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  2. T. V. Fomenko
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  3. I. K. Korobeinicheva
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  4. T. N. Gerasimova
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  5. E. P. Fokin
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1606–1611, July, 1980.

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Danilenko, N.I., Fomenko, T.V., Korobeinicheva, I.K. et al. Photochemical cyclization of anils of polyfluoroaromatic ketones. Russ Chem Bull 29, 1149–1154 (1980). https://doi.org/10.1007/BF00949173

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  • DOI: https://doi.org/10.1007/BF00949173

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