Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Molecular Iodine: A Versatile Catalyst for the Synthesis of 4-Aryl-3-methyl-1-phenyl-1H-benzo[h]pyrazolo[3,4-b]quinoline-5,10-diones in Water

  • Wu, Liqiang (School of Pharmacy, Xinxiang Medical University) ;
  • Yang, Limin (School of Pharmacy, Xinxiang Medical University) ;
  • Yan, Fulin (School of Pharmacy, Xinxiang Medical University) ;
  • Yang, Chung-Uang (School of Pharmacy, Xinxiang Medical University) ;
  • Fang, Lizhen (School of Pharmacy, Xinxiang Medical University)
  • Published : 2010.04.20
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References

  1. Devi, I.; Bhuyan, P. J. Tetrahedron Lett. 2004, 45, 8625. https://doi.org/10.1016/j.tetlet.2004.09.158
  2. El-Sayed, O. A.; Aboul-Enein, H. Y. Arch. Pharm. 2001, 334, 117. https://doi.org/10.1002/1521-4184(200104)334:4<117::AID-ARDP117>3.0.CO;2-9
  3. Wolin, R.; Wang, D.; Kelly, J.; Afonso, A.; James, L.; Kirschmeier,P.; Mcphail, A. T. Bioorg. Med. Chem. Lett. 1996, 6, 195. https://doi.org/10.1016/0960-894X(95)00574-D
  4. He, Z.; Milburn, G. H. W.; Baldwin, K. J.; Smith, D. A.; Danel,A.; Tomasik, P. J. Lumin. 2000, 86, 1. https://doi.org/10.1016/S0022-2313(99)00203-3
  5. Tomasik, P.; Tomasik, D.; Abramovitch, R. A. J. Heterocycl. Chem.1983, 20, 1539. https://doi.org/10.1002/jhet.5570200620
  6. Chaczatrian, K.; Chaczatrian, G.; Danel, A.; Tomasik, P. ARKIVOC2001, (vi), 63.
  7. Danel, A.; Chaczatrian, K.; Tomasik, P. ARKIVOC 2000, (i), 51.
  8. Quiroga, J.; Insuasty, B.; Saitz, C.; Jullian, C. J. Heterocycl. Chem.1998, 35, 575. https://doi.org/10.1002/jhet.5570350313
  9. Hua, G. P.; Xu, J. N.; Tu, S. J.; Wang, Q.; Zharlg, J. P.; Zhu, X. T.;Li, T. J.; Zhu, S. L.; Zhang, X. J. Chin. Org. Chem. 2005, 25, 1610.
  10. Lindstrom, U. M. Chem. Rev. 2002, 102, 2751. https://doi.org/10.1021/cr010122p
  11. Das, B.; Ravikanth, B.; Ramu, R.; Laxminarayana, K.; Rao, B.V. J. Mol. Catal. A: Chem. 2006, 255, 74 https://doi.org/10.1016/j.molcata.2006.04.007
  12. Kidwai, M.; Bansal,V.; Mothsra, P.; Saxena, S.; Somvanshi, R. K.; Dey, S.; Singh, T.P. J. Mol. Catal. A: Chem. 2007, 268, 76. https://doi.org/10.1016/j.molcata.2006.11.054
  13. Bhosale, R. S.; Magar,C. V.; Solanke, K. S.; Mane, S. B.; Choudhary, S. S.; Pawar, R.P. Synth. Commun. 2007, 37, 4353. https://doi.org/10.1080/00397910701578578

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