Diferrocenyl- and diferrocenylphenyl-acetonitriles

  • É. G. Perevalova
  • L. I. Leont'eva
  • M. D. Reshetova
Brief Communications
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Conclusions

  1. 1.

    Diferrocenylacetonitrile was prepared from the hydrochloride of diferrocenylchloromethane and from N-(diferrocenylmethyl)pyridinium p-toluenesulfonate. Diferrocenylphenylacetonitrile was prepared from the hydrochloride of diferrocenylphenylchloromethane.

     
  2. 2.

    Triferrocenylcarbinol, under conditions normally leading to the formation of N-(ferrocenylalkyl)-pyridinium salts, decomposes to diferrocenylfulvene.

     
  3. 3.

    Diferrocenylacetonitrile is transformed into diferrocenyl ketone on aluminum oxide.

     

Keywords

Oxide Aluminum Pyridinium Ketone Hydrochloride 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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Literature cited

  1. 1.
    A. N. Nesmeyanov, É. G. Perevalova, L. I. Leont'eva, and O. F. Filippov, Izv. AN SSSR, Ser. khim.,1967, 464.Google Scholar
  2. 2.
    A. N. Nesmeyanov, É. G. Perevalova, and M. D. Reshetova, Izv. AN SSSR, Ser. khim.,1966, 335.Google Scholar
  3. 3.
    A. N. Nesmeyanov, É. G. Perevalova, L. I. Leont'eva, and Yu. A. Ustynyuk, Izv. AN SSSR, Ser. khim.,1966, 558.Google Scholar
  4. 4.
    A. N. Nesmeyanov, É. G. Perevalova, L. I. Leont'eva, and Yu. A. Ustynyuk, Izv. AN SSSR, Ser. khim.,1966, 556.Google Scholar

Copyright information

© Consultants Bureau 1968

Authors and Affiliations

  • É. G. Perevalova
    • 1
  • L. I. Leont'eva
    • 1
  • M. D. Reshetova
    • 1
  1. 1.M. V. Lomonosov Moscow State UniversityUSSR

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