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Reaction Kinetics, Mechanisms and Catalysis

, Volume 102, Issue 1, pp 85–92 | Cite as

An effective and recyclable catalytic system for alcohol oxidation in water based on a temperature-responsive catalyst

  • Yong Ding
  • Wei Zhao
  • Yingshuai Zhang
  • Baochun Ma
  • Wenyuan Qiu
Article

Abstract

A facile and reusable catalytic system for alcohol oxidation with hydrogen peroxide was designed based on a temperature-responsive catalyst. Several kinds of alcohols were efficiently oxidized in high yields under relatively mild conditions. The catalyst could be easily recovered and reused.

Keywords

Alcohol Oxidation Temperature-responsive Catalyst Reusable 

Notes

Acknowledgements

This work was financially supported by the National Natural Science Foundation of China (Grant Nos. 20803032).

References

  1. 1.
    Fey T, Fischer H, Bachmann S, Albert K, Bolm C (2001) J Org Chem 66:8154CrossRefGoogle Scholar
  2. 2.
    Sheldon RA, Arends IWCE, Dijksman A (2000) Catal Today 57:157CrossRefGoogle Scholar
  3. 3.
    Singh RP, Subbarao HN, Dev S (1979) Tetrahedron 35:1789CrossRefGoogle Scholar
  4. 4.
    Clark JH (1999) Green Chem 1:1CrossRefGoogle Scholar
  5. 5.
    Sato K, Aokil M, Takagi J, Noyori R (1997) J Am Chem Soc 119:12386CrossRefGoogle Scholar
  6. 6.
    Ding Y, Zhao W, Hua H, Ma B (2008) Green Chem 10:910CrossRefGoogle Scholar
  7. 7.
    Zhao W, Ma B, Hua H, Zhang Y, Ding Y (2008) Catal Commun 9:2455CrossRefGoogle Scholar
  8. 8.
    Venturello C, Gambaro M (1991) J Org Chem 56:5924CrossRefGoogle Scholar
  9. 9.
    Ishii Y, Yamawaki K, Yoshida T, Ura T, Ogawa M (1987) J Org Chem 52:1868CrossRefGoogle Scholar
  10. 10.
    Bamoharram FF, Roshani M, Heravi MM, Safaie S (2006) Phosphorus Sulfur Silicon Relat Elem 181:2833CrossRefGoogle Scholar
  11. 11.
    Carraro M, Sandei L, Sartorel A, Scorrano G, Bonchio M (2006) Org Lett 8:3671CrossRefGoogle Scholar
  12. 12.
    Sato K, Hyodo M, Aoki M, Zheng X-Q, Noyori R (2001) Tetrahedron 57:2469CrossRefGoogle Scholar
  13. 13.
    Sloboda-Rozner D, Alsters PL, Neumann R (2003) J Am Chem Soc 125:5280CrossRefGoogle Scholar
  14. 14.
    Sloboda-Rozner D, Witte P, Alsters PL, Neumann R (2004) Adv Synth Catal 346:339CrossRefGoogle Scholar
  15. 15.
    Wang J, Yan L, Li G, Wang X, Ding Y, Suo J (2005) Tetrahedron Lett 46:7023CrossRefGoogle Scholar
  16. 16.
    Zhao W, Zhang Y, Ma B, Ding Y, Qiu W (2010) Catal Commun 11:527CrossRefGoogle Scholar
  17. 17.
    Ma B, Zhang Y, Ding Y, Zhao W (2010) Catal Commun 11:853CrossRefGoogle Scholar
  18. 18.
    Hamamoto H, Suzuki Y, Yamada YMA, Tabata H, Takahashi H, Ikegami S (2005) Angew Chem Int Ed 44:4536CrossRefGoogle Scholar
  19. 19.
    Lambert A, Plucinskib P, Kozhevnikov IV (2003) Chem Commun 714Google Scholar
  20. 20.
    Kaur J, Kozhevnikov IV (2004) Catal Commun 5:709CrossRefGoogle Scholar
  21. 21.
    Li C, Gao J, Jiang Z, Wang S, Lu H, Yang Y, Jing F (2005) Top Catal 35:169CrossRefGoogle Scholar
  22. 22.
    Li J, Zhang Y, Han D, Jia G, Gao J, Zhong L, Li C (2008) Green Chem 10:608CrossRefGoogle Scholar
  23. 23.
    Li C, Jiang Z, Gao J, Yang Y, Wang S, Tian F, Sun F, Sun X, Ying P, Han C (2004) Chem Eur J 10:2277CrossRefGoogle Scholar
  24. 24.
    Tézé A, Hervé G (1990) Inorg Synth 27:85CrossRefGoogle Scholar

Copyright information

© Akadémiai Kiadó, Budapest, Hungary 2010

Authors and Affiliations

  • Yong Ding
    • 1
  • Wei Zhao
    • 1
  • Yingshuai Zhang
    • 1
  • Baochun Ma
    • 1
  • Wenyuan Qiu
    • 1
  1. 1.State Key Laboratory of Applied Organic ChemistryCollege of Chemistry and Chemical Engineering, Lanzhou UniversityLanzhouChina

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