Skip to main content
Log in

Use of ferrocenyl chelated palladacycles as catalysts for the Heck reaction

  • Full Articles
  • Published:
Russian Chemical Bulletin Aims and scope

Abstract

Two ferrocenyl palladacycles with bi-and tridentate (C,N) and (C,N,N) ligands were tested as possible catalysts for the Heck reaction. The latter complex efficiently catalyzed reactions of aryl halides with ethyl acrylate.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Y. J. Wu, J. Hou, H. Yun, X. Cui, R. Yuan, J. Organomet. Chem., 2001, 637–639, 793.

    Article  Google Scholar 

  2. C. Hu, J. F. Gong, S. F. Yue, Y. J. Wu, J. Chem. Soc., Dalton Trans., 2006, 4730.

  3. B. Mu, T. Li, W. Hu, G. Zeng, P. Liu, Y. J. Wu, Tetrahedron, 2007, 63, 11475.

    Article  CAS  Google Scholar 

  4. L. L. Troitskaya, V. I. Sokolov, O. A. Reutov, Dokl. Akad. Nauk SSSR, 1979, 246, 124 [Dokl. Chem. (Engl. Transl.), 1979, 246].

    Google Scholar 

  5. N. S. Khrushcheva, V. I. Sokolov, Izv. Akad. Nauk, Ser. Khim., 2006, 1116 [Russ. Chem. Bull., Int. Ed., 2006, 55, 1159].

  6. L. A. Bulygina, V. I. Sokolov, I. A. Utepova, V. L. Rusinov, O. N. Chupakhin, Izv. Akad. Nauk, Ser. Khim., 2007, 1039 [Russ. Chem. Bull., Int. Ed., 2007, 56, 1080].

    Google Scholar 

  7. V. I. Sokolov, L. L. Troitskaya, O. A. Reutov, J. Organomet. Chem., 1979, 182, 537.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to V. I. Sokolov.

Additional information

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1370–1372, July, 2010.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sokolov, V.I., Bulygina, L.A., Khrushcheva, N.S. et al. Use of ferrocenyl chelated palladacycles as catalysts for the Heck reaction. Russ Chem Bull 59, 1400–1402 (2010). https://doi.org/10.1007/s11172-010-0253-6

Download citation

  • Received:

  • Revised:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11172-010-0253-6

Navigation