10.1186/2228-5326-3-49

Synthesis of quinoline derivatives from the reaction of aminobenzophenones and acetylenic esters in the presence of SnO2 nanoparticles

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  • Mohammad Qandalee*1,
  • Mohammad Alikarami2,
  • Hossein Mighani3,
  • Sakineh Asghari4,
  • Shahin Beikjani5,
  • Mehdi Hatami6,
  1. Department of biology, Garmsar branch, Islamic Azad University, Garmsar, IR
  2. Department of Chemistry, Ilam Branch, Islamic Azad University, Ilam, IR
  3. Department of Chemistry, Faculty of science, Golestan University, Gorgan, IR
  4. Department of Chemistry, Ayatollah Amoli Branch, Islamic Azad University, Amol, IR
  5. Department of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, 47416, IR
  6. Department of Marine Chemistry, Faculty of Marine Science, Khorramshahr University of Marine Science and Technology, Khorramshahr, IR
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Published in Issue 2013-08-23

How to Cite

Qandalee, M., Alikarami, M., Mighani, H., Asghari, S., Beikjani, S., & Hatami, M. (2013). Synthesis of quinoline derivatives from the reaction of aminobenzophenones and acetylenic esters in the presence of SnO2 nanoparticles. International Nano Letters, 3(1 (December 2013). https://doi.org/10.1186/2228-5326-3-49
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Abstract

Abstract Nano SnO 2 catalyzes the two-component reaction of 2-aminobenzophenones with acetylenic mono or diesters under mild conditions to afford quinoline derivatives in high yields. Nano SnO 2 shows high activity when used as surface catalyst for the synthesis of quinoline derivatives.

Keywords

  • Nano SnO2,
  • Acetylenic esters,
  • Quinoline,
  • 2-Aminobenzophenones
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References

  1. Corma and Serna (2006) Chemoselective Hydrogenation of Nitro Compounds with Supported Gold Catalysts https://doi.org/10.1126/science.1128383
  2. Enache et al. (2006) https://doi.org/10.1126/science.1120560
  3. Hughes et al. (2005) https://doi.org/10.1038/nature04190
  4. Liang et al. (2004) https://doi.org/10.1002/anie.200352956
  5. Astruc et al. (2005) https://doi.org/10.1002/anie.200500766
  6. Valden et al. (1998) https://doi.org/10.1126/science.281.5383.1647
  7. Huang et al. (2004) https://doi.org/10.1002/anie.200352682
  8. Li and Bi (2007)
  9. El-Etre and Reda (2010) https://doi.org/10.1016/j.apsusc.2010.04.055
  10. Li et al. (2010) https://doi.org/10.1016/j.jpowsour.2009.11.005
  11. Arpita et al. (2010) https://doi.org/10.1016/j.molcata.2010.05.015
  12. Modou and Roy (1989) Academic Press
  13. Barton and Ollis (1979) (pp. 166-203) Pergamon
  14. Desai et al. (1996)
  15. Sonza and Vasconcelos (2005) https://doi.org/10.1590/S0100-40422005000400022
  16. Hirano et al. (2002) https://doi.org/10.1248/jhs.48.118
  17. Larsen et al. (1996) https://doi.org/10.1021/jo952103j
  18. Chen et al. (2001) 44(K.C Fang) https://doi.org/10.1021/jm0100335
  19. Kallmaya and Serrnivasa (1998) https://doi.org/10.1016/S0014-827X(98)00037-8
  20. Ko et al. (2001) https://doi.org/10.1016/S0960-894X(00)00652-1
  21. Ferrarini et al. (1997) https://doi.org/10.1002/jhet.5570340520
  22. Maguire et al. (1994) https://doi.org/10.1021/jm00040a003
  23. Bergstrom (1944) https://doi.org/10.1021/cr60111a001
  24. Edward (1966) https://doi.org/10.1021/jo01347a038
  25. Jones (1997) (pp. 93-318) Wiley
  26. Reitsema (1948) https://doi.org/10.1021/cr60134a002
  27. Jones et al. (1996) Pergamon
  28. Asghari et al. (2010) https://doi.org/10.1007/s11030-009-9188-y