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An Efficient Method for the Sulfonylation of Aromatic Rings with Arene/Alkane Sulfonic Acid by Using P2O5/SiO2 under Heterogeneous Conditions

  • 발행 : 2003.07.20

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참고문헌

  1. Jensen, F. R.; Goldman, G. In Friedel-Crafts and RelatedReaction; Olah, G., Ed.; Wiley Intrscience: New York, 1964;V.III, pp 1319-1367.
  2. Simpkins, N. S. Sulfones in OrganicSynthesis; Pergamon Press: Oxford, 1993.
  3. Roy, K. M. In Ullmann's Encyclopedia of Industrial Chemistry;Gerhartz, W., Ed.; VCH: Weinheim, 1985; V.A 25, pp 487-501.
  4. Hastings, R. C.; Franzblau, S. G. Ann. Rev. Pharmacol. Toxicol.1966, 28, 231. https://doi.org/10.1146/annurev.pa.28.040188.001311
  5. Wozel, G. Int. J. Dermatol. 1989, 28, 17. https://doi.org/10.1111/j.1365-4362.1989.tb01301.x
  6. Frost, C. G.; Hartley, J. P.; Griffin, D. Tetrahedron Lett. 2002, 43,4789. https://doi.org/10.1016/S0040-4039(02)00931-0
  7. Singh, R. P.; Kamble, R. M.; Chandra, K. L.; Saravanane, P.;Singh, V. K. Tetrahedron 2001, 57, 241. https://doi.org/10.1016/S0040-4020(00)01005-X
  8. Olah, G. A.; Mathew, T.; Parakash, G. K. S. Chem. Commun.2001, 1969.
  9. Zolfigol, M. A. Tetrahedron 2001, 57, 9509 and other ourreferences cited therein. https://doi.org/10.1016/S0040-4020(01)00960-7
  10. Zolfigol, M. A.; Torabi, M.;Mallakpour, S. E. Tetrahedron 2001, 57, 8381. https://doi.org/10.1016/S0040-4020(01)00832-8
  11. Zolfigol, M.A.; Zebarjadian, M. H.; Chehardoli, G.; Mallakpour, S. E.;Shamsipur, M. Tetrahedron 2001, 57, 1627. https://doi.org/10.1016/S0040-4020(00)01150-9
  12. Zolfigol, M. A.;Bamoniri, A. Synlett 2002, 1621.
  13. Zolfigol, M. A.; Ghorbani-Choghamarani, A.; Hazarkhani, H. Synlett 2002, 1002.
  14. Zolfigol, M. A.; Madrakian, E.; Ghaemi, E.; Mallakpour, S. E.Synlett 2002, 1633.
  15. March, J. Advanced Organic Chemistry, 3rd Ed.; John Wiley:New York, 1985; p 904.
  16. Eaton, C. L. J. Org. Chem. 1973, 38, 4071. https://doi.org/10.1021/jo00987a028
  17. Eshghi, H.; Rafei, M.; Karimi, M. H. Synth. Commun. 2001, 31, 771. https://doi.org/10.1081/SCC-100103268

피인용 문헌

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  2. Sulfonylation of aromatic compounds with methyl p-toluenesulfonate as a sulfonylating precursor vol.9, pp.4, 2012, https://doi.org/10.1007/s13738-011-0062-3
  3. Upward Trend in Catalytic Efficiency of Rare-Earth Triflate Catalysts in Friedel-Crafts Aromatic Sulfonylation Reactions vol.3, pp.9, 2014, https://doi.org/10.1002/ajoc.201402067
  4. An Efficient Method for the Sulfonylation of Aromatic Rings with Arene/Alkane Sulfonic Acid by Using P2O5/SiO2 under Heterogeneous Conditions. vol.34, pp.52, 2003, https://doi.org/10.1002/chin.200352094
  5. An efficient conversion of β-diketones into β-keto enol ethers with P2O5/SiO2 under solvent-free conditions vol.2006, pp.6, 2006, https://doi.org/10.3184/030823406777946815
  6. Rapid and mild sulfonylation of aromatic compounds with sulfonic acids via mixed anhydrides using Tf2O vol.48, pp.38, 2003, https://doi.org/10.1016/j.tetlet.2007.07.081
  7. Sulfonylation of aromatic compounds with sulfonic acids using silica gel-supported AlCl3as a heterogeneous Lewis acid catalyst vol.31, pp.3, 2003, https://doi.org/10.1080/17415991003777391
  8. Polystyrene Supported Al(OTf)3: a Stable, Efficient, Selective, and Reusable Catalyst for Sulfonylation of Arenes with Sulfonic Acids vol.31, pp.7, 2010, https://doi.org/10.5012/bkcs.2010.31.7.1887
  9. Direct Metal‐ and Reagent‐Free Sulfonylation of Phenols with Sodium Sulfinates by Electrosynthesis vol.25, pp.28, 2019, https://doi.org/10.1002/chem.201900850
  10. Straightforward Electrochemical Sulfonylation of Arenes and Aniline Derivatives using Sodium Sulfinates vol.6, pp.17, 2003, https://doi.org/10.1002/celc.201901212
  11. Recent Progress and Emerging Technologies towards a Sustainable Synthesis of Sulfones vol.14, pp.22, 2003, https://doi.org/10.1002/cssc.202101635