Advertisement

Russian Journal of Physical Chemistry A

, Volume 93, Issue 1, pp 34–38 | Cite as

Ligands Based on 2,3,6-O-Cellulose Derivatives for Catalysts of Asymmetric Hydrogenation

  • N. D. ZubarevaEmail author
  • D. V. Kurilov
  • E. I. Klabunovskii
  • A. Yu. Stakheev
  • L. M. Kustov
CHEMICAL KINETICS AND CATALYSIS

Abstract

Means of synthesis are developed and a physicochemical study of ligands based on 2,3,6-О-cellulose derivatives for asymmetric hydrogenation catalysts is performed.

Keywords:

asymmetric hydrogenation catalysts synthesis methods 2,3,6-О-cellulose derivatives 

Notes

ACKNOWLEDGMENTS

We are grateful to E.N. Rasadkina for supplying the sample of 2,2'-dihydroxy-3-carboxy-1,1'-binaphthyl. This work was supported by the Russian Science Foundation, project no. 14-50-00126.

REFERENCES

  1. 1a.
    J. Zvacek, Czech. Patent No. 107120 (1964);Google Scholar
  2. 1b.
    Chem. Abstr. 59, 14632h (1963).Google Scholar
  3. 2.
    K. Harada and T. Yoshida, Naturwissensch. 57, 131 (1970).CrossRefGoogle Scholar
  4. 3.
    H. Pracejus and M. Bursian, Ger. Patent No. 92031 (1972), Chem. Abstr. 78, 72591b (1973).Google Scholar
  5. 4.
    Y. Kawabata, M. Tanaka, and I. Ogata, Chem. Lett., 1213 (1976).Google Scholar
  6. 5.
    K. Kaneda, H. Yamamoto, T. Imanaka, and Sh. Teranishi, J. Mol. Catal. 29, 99 (1985).CrossRefGoogle Scholar
  7. 6.
    T. Minuth and M. K. Boysen Mike, Org. Lett. 11, 4212 (2009).CrossRefGoogle Scholar
  8. 7.
    H. Grugel, T. Minuth, and M. K. Boysen Mike, Synthesis 19, 3248 (2010).Google Scholar
  9. 8.
    P. Tian, H-Q. Dong, and G-Q. Lin, ACS Catal. 2, 95 (2012).CrossRefGoogle Scholar
  10. 9.
    B. R. Harkness and D. G. Gray, Macromolecules 23, 1452 (1990).CrossRefGoogle Scholar
  11. 10.
    J. Honeyman, J. Chem. Soc., 168 (1947).Google Scholar
  12. 11.
    F. F. L. Ho and D. W. Klosiewicz, Anal. Chem. 52, 913 (1980).CrossRefGoogle Scholar
  13. 12.
    Methods in Carbohydrate Chemistry, Vol. 3: Cellulose, Ed. by R. Whistler (Academic, New York, 1963), pp. 4, 27, 327.Google Scholar
  14. 13.
    C. Chassaing, A. Thienpont, and G. Felix, J. Chromatogr., A 738, 157 (1996).Google Scholar
  15. 14.
    Y. Kaida and Y. Okamoto, Bull. Chem. Soc. Jpn. 66, 2225 (1993).CrossRefGoogle Scholar
  16. 15.
    V. P. Ananikov, E. G. Gordeev, M. P. Egorov, et al., Mendeleev Commun. 26, 365 (2016).CrossRefGoogle Scholar
  17. 16.
    V. P. Ananikov, L. M. Kustov, A. L. Tarasov, et al., Mendeleev Commun. 27, 425 (2017).CrossRefGoogle Scholar

Copyright information

© Pleiades Publishing, Ltd. 2019

Authors and Affiliations

  • N. D. Zubareva
    • 1
    Email author
  • D. V. Kurilov
    • 1
  • E. I. Klabunovskii
    • 1
  • A. Yu. Stakheev
    • 1
  • L. M. Kustov
    • 1
  1. 1.N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of SciencesMoscowRussia

Personalised recommendations