Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

H3PW12O40-SoiO2 and Amberlyst 15: Two Efficient Heterogeneous Catalysts for Synthesis of N-Acylsulfonamides under Solvent-free Conditions

  • Wu, Liqian (School of Pharmacy, Xinxiang Medical University) ;
  • Yang, Chunguang (School of Pharmacy, Xinxiang Medical University) ;
  • Zhang, Chong (School of Pharmacy, Xinxiang Medical University) ;
  • Yang, Limin (School of Pharmacy, Xinxiang Medical University)
  • Published : 2009.07.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Hasegawa, T.; Yamamoto, H. Bull. Chem. Soc. Jpn. 2000, 73, 423 https://doi.org/10.1246/bcsj.73.423
  2. Massah, A. R.; Adibi, H.; Khodarahmi, K.; Abiri, R.; Majnooni, M. B.; Shahidi, S.; Asadi, B.; Mehrabi, M.; Zolgol, M. A. Bioorg. Med. Chem. 2008, 16, 5465 https://doi.org/10.1016/j.bmc.2008.04.011
  3. Chang, L. L.; Ashton, W. T.; Flanagan, K. L.; Chen, T. B.; O'Malley, S. S.; Zingaro, G. J.; Siegl, P. K. S.; Kivlighn, S. D.; Lotti, V. J.; Chang, R. S. L.; Greenless, W. J. J. Med. Chem. 1994, 37, 4464 https://doi.org/10.1021/jm00052a006
  4. Musser, J. H.; Kreft, A. F.; Bender, R. H. W.; Kubrak, D. M.; Grimes, D.; Carlson, R. P.; Hand, J. M.; Chang, J. J. Med. Chem. 1990, 33, 240 https://doi.org/10.1021/jm00163a039
  5. Kondo, K.; Sekimoto, E.; Miki, K.; Murakami, Y. J. Chem. Soc. Perkin Trans. 1 1998, 2973
  6. Martin, M. T.; Roschangar, F.; Eaddy, J. F. Tetrahedron Lett. 2003, 44, 5461 https://doi.org/10.1016/S0040-4039(03)01324-8
  7. Reddy, C. R.; Mahipal, B.; Yaragorla, S. R. Tetrahedron Lett. 2007, 48, 7528 https://doi.org/10.1016/j.tetlet.2007.08.048
  8. Singh, D. U.; Singh, P. R.; Samant, S. D. Tetrahedron Lett. 2004, 45, 4805 https://doi.org/10.1016/j.tetlet.2004.04.077
  9. Massah, A. R.; Momeni, A. R.; Dabagh, M. Synth. Commun. 2007, 38, 265 https://doi.org/10.1080/00397910701750185
  10. Wang, Y.; Soper, D. L.; Dirr, M. J.; Delong, M. A.; De, B.; Wos, J. A. Chem. Pharm. Bull. 2000, 48, 1332 https://doi.org/10.1248/cpb.48.1332
  11. Clark, J. H. Acc. Chem. Res. 2002, 35, 791 https://doi.org/10.1021/ar010072a
  12. Mirjalili, B. B. F.; Zaghaghi, Z. J. Chin. Chem. Soc. 2008, 55, 694
  13. Meuzelaar, G.; Maat, L.; Sheldon, R.; Kozhevnikov, I. V. Catal. Lett. 1997, 45, 249 https://doi.org/10.1023/A:1019052604032
  14. Kozhevnikova, E. F.; Rafiee, E.; Kozhevnikov, I. V. Appl. Catal. 2004, A260, 25
  15. Mao, J.; Nakajo, T.; Okuhara, T. Chem. Lett. 2002, 1104
  16. Das, B.; Banerjee, J. Chem. Lett. 2004, 33, 960 https://doi.org/10.1246/cl.2004.960
  17. Ramesh, C.; Banerjee, J. R.; Pal, B. D. Adv. Synth. Catal. 2002, 345, 557 https://doi.org/10.1002/adsc.200303022
  18. Feng, X.-L.; Guan, C.-J.; Zhao, C.-X. Synth. Commum. 2004, 34, 487 https://doi.org/10.1081/SCC-120027288
  19. Farhanullah.; Ashoke, S.; Maulik, P. R.; Ram V. J. Tetrahedron Lett. 2004, 45, 5099 https://doi.org/10.1016/j.tetlet.2004.04.172
  20. Solladie-Cavallo, A.; Lupattelli, P.; Bonini, C. J. Org. Chem. 2005, 70, 1605 https://doi.org/10.1021/jo048045w
  21. Das, B.; Thirupathi, P.; Mahender, I.; Reddy, V. S.; Rao, Y. K. J. Mol. Catal. A: Chem. 2006, 255, 233
  22. Ko, S.-K.; Yao, C.-F. Tetrahedron Lett. 2006, 47, 8827 https://doi.org/10.1016/j.tetlet.2006.10.072
  23. Yijima, C.; Hino, F.; Suda, K. Synthesis 1981, 610
  24. Oh, S. W. J. Photosci. 2005, 12, 63

Cited by

  1. -sulfonyl imines vol.31, pp.6, 2010, https://doi.org/10.1080/17415993.2010.521940
  2. FeCl3–SiO2 as heterogeneous catalysts for the preparation of dihydropyrano[3,2-b]chromenediones vol.76, pp.12, 2012, https://doi.org/10.1135/cccc2011108
  3. -acyl sulfonamides and cyclic imides pp.1532-2432, 2018, https://doi.org/10.1080/00397911.2018.1535077
  4. ChemInform Abstract: H3PW12O40-SiO2 and Amberlyst 15: Two Efficient Heterogeneous Catalysts for Synthesis of N-Acylsulfonamides under Solvent-Free Conditions. vol.40, pp.51, 2009, https://doi.org/10.1002/chin.200951103
  5. Synthesis and structural study of N-acetyl-1,2,3,4-tetrahydroisoquinoline-2-sulfonamide obtained using H6P2W18O62 as acidic solid catalyst vol.1041, pp.None, 2009, https://doi.org/10.1016/j.molstruc.2013.02.018