Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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A Mild, Efficient and Eco-friendly Synthesis of 1,3-Bis(4-arylthiazol-2-yl)benzenes in PEG-400

  • Noei, Jalil (Catalysis Division, Department of Chemistry, Faculty of Science, University of Isfahan) ;
  • Khosropour, Ahmad Reza (Catalysis Division, Department of Chemistry, Faculty of Science, University of Isfahan)
  • Received : 2009.08.02
  • Accepted : 2010.04.10
  • Published : 2010.11.20
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Abstract

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References

  1. Roje, S. Phytochem. 2007, 68, 1904. https://doi.org/10.1016/j.phytochem.2007.03.038
  2. Shatursky, O. Y.; Volkova, T. M.; Romanenko, O. V.; Himmelreich, N. H.; Grishin, E. V. Biochim Biophys. Acta 2007, 1768, 207. https://doi.org/10.1016/j.bbamem.2006.10.012
  3. Lawton, G., Witty, D. R., Eds.; Progress in Medicinal Chemistry; Vol. 46, Elsevier Science: 2008.
  4. Harmata, M., Stork, G., Eds.; Strategies and Tactics in Organic Synthesis; Vol. 7, Academic Press: 2008.
  5. Lednicer, D. The Organic Chemistry of Drug Synthesis; Wiley-Interscience: New York, 2007.
  6. Franklin, P. X.; Pillai, A. D.; Rathod, P. D.; Yerande, S.; Nivsarkar, M.; Padh, H.; Vasu, K. K.; Sudarsanam, V. Eur. J. Med. Chem. 2008, 43, 129. https://doi.org/10.1016/j.ejmech.2007.02.008
  7. Jain, K. S.; Bariwal, J. B.; Kathiravan, M. K.; Phoujdar, M. S.; Sahne, R. S.; Chauhan, B. S.; Shah, A. K.; Yadav, M. R. Bioorg. Med. Chem. 2008, 16, 4759. https://doi.org/10.1016/j.bmc.2008.02.091
  8. Hyland, L.; Villarreal-Ramos, B.; Clarke, B.; Baaten, B.; Hou, S. Exp. Hematol. 2005, 33, 1477. https://doi.org/10.1016/j.exphem.2005.09.005
  9. Romagnoli, R.; Baraldi, P. G.; Lopez, O. C.; Carrion, M. D.; Cara1, C. L.; Preti1, D.; Tabrizi, M. A.; Balzarini, J. Lett. Drug Des. Discov. 2007, 4, 464. https://doi.org/10.2174/157018007781788507
  10. Delbecq, F.; Cordonnier, G.; Pommery, N.; Barbry, D.; Hénichart,J.-P. J. Med. Chem. 2004, 14, 1119.
  11. Metzger, J. V. Comprehensive Heterocyclic Chemistry; Katritzky,R., Rees, C. W., Eds.; Pergamon: New York, NY, 1984; Vol. 6, p 235.
  12. Eckensta, J.; Brogle, E.; Storkin, E.; Erlenmeyer, H.; Helv. Chem. Acta. 1950, 33, 1353. https://doi.org/10.1002/hlca.19500330535
  13. Varma, R. S.; Kumar, D.; Liesen, P. J. J. Chem. Soc. Perkin Trans 1 1998, 4093.
  14. Narender, M.; Somi Reddy, M.; Sridhar, R.; Nageswar, Y. V. D.; Rama Rao, K. Tetrahedron Lett. 2005, 46, 5953. https://doi.org/10.1016/j.tetlet.2005.06.130
  15. Das, B.; Saidi Reddy, V.; Ramu, R. J. Mol. Catal. A: Chem. 2006, 252, 235. https://doi.org/10.1016/j.molcata.2006.02.065
  16. Siddiqui, H. L.; Iqbal, A.; Ahmed, S.; Weaver, G. Molecules 2006,11, 206. https://doi.org/10.3390/11020206
  17. George, W. K.; Arjun, R. M. Tetrahedron Lett. 2006,47, 5171. https://doi.org/10.1016/j.tetlet.2006.05.053
  18. Karade, H.; Sathe, M.; Kaushik, M. P. Catal. Commun. 2007, 8, 741. https://doi.org/10.1016/j.catcom.2006.09.005
  19. Koichi, M. Green Reaction Media for Organic Synthesis; Blackwell:Oxford, 2005.
  20. Khosropour, A. R.; Khodaei, M. M.; Hoseini Jomor, S. J. Heterocycl. Chem. 2008, 45, 683. https://doi.org/10.1002/jhet.5570450308
  21. Khosropour, A. Ultrason. Sonochem. 2008, 15, 659. https://doi.org/10.1016/j.ultsonch.2007.12.005
  22. Khosropour, A. R.; Mohammadpoor-Baltork, I.; Ghorbankhani, H. Tetrahedron Lett. 2006, 47, 3561. https://doi.org/10.1016/j.tetlet.2006.03.079
  23. Khosropour, A. R. Can. J. Chem. 2008, 86, 264. https://doi.org/10.1139/V08-009
  24. Noei, J.; Khosropour, A. R. Tetrahedron Lett. 2008, 49, 6969. https://doi.org/10.1016/j.tetlet.2008.09.084
  25. Noei, J.; Khosropour, A. R. Ultrason. Sonochem. 2009, 16, 711. https://doi.org/10.1016/j.ultsonch.2009.04.001

Cited by

  1. ChemInform Abstract: A Mild, Efficient and Eco-Friendly Synthesis of 1,3-Bis(4-arylthiazol-2-yl)benzenes in PEG-400. vol.42, pp.13, 2011, https://doi.org/10.1002/chin.201113109