Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Tf2O-Mediated Direct and Regiospecific para-Acylation of Phenols with Carboxylic Acids

  • Khodaei, M.M. (Faculty of Chemistry and Nanoscience & Nanotechnology Research Center (NNRC), Razi University) ;
  • Nazari, E. (Faculty of Chemistry and Nanoscience & Nanotechnology Research Center (NNRC), Razi University)
  • Received : 2011.01.31
  • Accepted : 2011.03.07
  • Published : 2011.05.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Fritch, J.; Fruchey, O.; Horlenko, T. US patent 4954652, Hoechst Celanese Corporation 1990.
  2. Crouse, D. J.; Hurlbut, S. L.; Wheeler, D. M. S. J. Org. Chem. 1981, 46, 374. https://doi.org/10.1021/jo00315a028
  3. Martin, R. Org. Prep. Proced. Int. 1992, 24, 369. https://doi.org/10.1080/00304949209356226
  4. Olah, G. A. Friedel-Crafts and Related Reactions; Wiley Interscience: New York, NYand London, 1963-1964; Vols. I-IV.
  5. Hocking, M. B. J. Chem. Technol. Biotechnol. 1980, 30, 626.
  6. Ramesh, B. B. IN 171 970 (February 1993), Shasun Chemicals (m) Ltd., India.
  7. Boyer, J. L. J. Org. Chem. 2000, 62, 4712.
  8. Martin, R. Org. Prep. Proc. Int. 1992, 24, 369. https://doi.org/10.1080/00304949209356226
  9. Heidekum, A. J. Catal. 1998, 176, 260. https://doi.org/10.1006/jcat.1998.2034
  10. Mueller, J.; Wiersdorff, W.; Kirschenlohr, W.; Schwantje, G. US patent 4508924, BASF 1985.
  11. Mott, G. N. US patent 4607125, Celanese Corporation, 1986.
  12. Effenberger, F. Angew. Chem. 1980, 92, 147. https://doi.org/10.1002/ange.19800920304
  13. Martinez, A. G.; Fernandez, H. A.; Vilches, M. D.; Gutierrez, L. L.; Subramanian, L. R. Synlett. 1993, 229.
  14. Baraznenok, I. L.; Nenajdenko, V. G.; Balenkova, E. S. Tetrahedron 2000, 56, 3077. https://doi.org/10.1016/S0040-4020(00)00093-4
  15. Salehi, P.; Khodaei, M. M.; Zolfigol, M. A.; Sirouszadeh, S. Bull. Chem. Soc. Jpn. 2003, 76, 1863. https://doi.org/10.1246/bcsj.76.1863
  16. Salehi, P.; Khodaei, M. M.; Zolfigol, M. A.; Zeinoldini, S. Synth. Commun. 2003, 33, 1367. https://doi.org/10.1081/SCC-120018697
  17. Alizadeh, A.; Khodaei, M. M.; Nazari, E. Bull. Korean Chem. Soc. 2007, 28, 1854. https://doi.org/10.5012/bkcs.2007.28.10.1854
  18. Bahrami, K.; Khodaei, M. M.; Shahbazi, F. Chem. Lett. 2008, 37, 844. https://doi.org/10.1246/cl.2008.844
  19. Khodaei, M. M.; Alizadeh, A.; Nazari, E. Tetrahedron Lett. 2007, 48, 4199. https://doi.org/10.1016/j.tetlet.2007.04.066
  20. Alizadeh, A.; Khodaei, M. M.; Nazari, E. Tetrahedron Lett. 2007, 48, 4805. https://doi.org/10.1016/j.tetlet.2007.05.076
  21. Bahrami, K.; Khodaei, M. M.; Karimi, A. Synthesis 2008, 1682.
  22. Bahrami, K.; Khodaei, M. M.; Karimi, A. Synthesis 2008, 2543.
  23. Khodaei, M. M.; Nazari, E. Chem. Lett. 2010, 39, 390. https://doi.org/10.1246/cl.2010.390
  24. Weast, R. C. Handbook of Chemistry and Physic, 55th ed.; CRC Press: Ohio, 1974.
  25. Buckingham, J.; MacDonald, F. Dictionary of Organic Compounds; 6th Ed.; Chapman and Hall: London, 1996.

Cited by

  1. ChemInform Abstract: Tf2O-Mediated Direct and Regiospecific para-Acylation of Phenols with Carboxylic Acids. vol.42, pp.43, 2011, https://doi.org/10.1002/chin.201143070
  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. Synthesis and Evaluation of Some Phenol-Based Anionic Gemini Amphiphiles: Studying Their Influence in the Preparation of Cu2O nanoparticles vol.53, pp.2, 2011, https://doi.org/10.3139/113.110419