Bulletin of the Korean Chemical Society

  • 제31권4호
  • /
  • Pages.1051-1054
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  • 2010
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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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)
  • 발행 : 2010.04.20
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참고문헌

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  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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  1. l-Proline-catalysed sequential four-component “on water” protocol for the synthesis of structurally complex heterocyclic ortho-quinones vol.13, pp.11, 2011, https://doi.org/10.1039/c1gc15794a
  2. An iodine-mediated green synthesis of 1,3,4-oxadiazoles under solvent-free conditions using grinding technique vol.4, pp.1, 2011, https://doi.org/10.1080/17518253.2010.502909
  3. PEG1000-Based Dicationic Acidic Ionic Liquid Catalyzed One-Pot Synthesis of 4-Aryl-3-Methyl-1-Phenyl-1H-Benzo[h]pyrazolo [3,4-b]quinoline-5,10-Diones via Multicomponent Reactions vol.5, pp.4, 2015, https://doi.org/10.3390/catal5041649
  4. Lawsone in organic synthesis vol.5, pp.83, 2015, https://doi.org/10.1039/C5RA12785H
  5. ]quinoline Hybrid Heterocycles vol.18, pp.5, 2016, https://doi.org/10.1021/acscombsci.6b00003
  6. Recent Developments in the Synthesis of Five- and Six-Membered Heterocycles Using Molecular Iodine vol.18, pp.18, 2012, https://doi.org/10.1002/chem.201100324
  7. Synthesis of Biologically Relevant Heterocycles in Aqueous Media vol.7, pp.10, 2018, https://doi.org/10.1002/ajoc.201800396
  8. Recent Progress in the Synthesis of Pyrazolopyridines and Their Derivatives pp.1945-5453, 2019, https://doi.org/10.1080/00304948.2018.1542517
  9. Iodine-catalyzed transformation of molecules containing oxygen functional groups vol.67, pp.7, 2011, https://doi.org/10.1016/j.tet.2010.11.086
  10. Molecular iodine-catalyzed multicomponent reactions: an efficient catalyst for organic synthesis vol.3, pp.20, 2010, https://doi.org/10.1039/c3ra23461d
  11. L-proline catalyzed multicomponent reactions: facile access to 2H-benzo[g]pyrazolo[3,4-b]quinoline-5,10(4H,11H)-dione derivatives vol.4, pp.29, 2010, https://doi.org/10.1039/c4ra00876f
  12. Recent Synthetic Approaches and Biological Evaluations of Amino Hexahydroquinolines and Their Spirocyclic Structures vol.19, pp.7, 2010, https://doi.org/10.2174/1871520619666190131140436
  13. Recent Advances on Diversity Oriented Heterocycle Synthesis of Fused Quinolines and Its Biological Evaluation vol.41, pp.10, 2010, https://doi.org/10.1080/10406638.2019.1710856