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Rapid and Efficient Method for Room Temperature Deoximation Reaction Under Solvent-Free Conditions

  • Dewan, Anindita (Department of Chemistry, Gauhati University) ;
  • Bora, Utpal (Department of Chemistry, Dibrugarh University) ;
  • Kakati, Dilip K. (Department of Chemistry, Gauhati University)
  • Received : 2011.04.27
  • Accepted : 2011.06.01
  • Published : 2011.07.20
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Abstract

Keywords

References

  1. Greene, T. W.; Wuts, P. G. M. In Protective Groups in Organic Synthesis; Wiley: New York, 1991; p 214.
  2. Donaruma, L. G.; Heltd, W. Z. Organic Reactions 1960, 11, 1.
  3. Kabalka, G. W.; Pace, R. D.; Wadgaonkar, P. P. Synth Commun. 1990, 20, 2453. https://doi.org/10.1080/00397919008053193
  4. Barton, D. H. R.; Beaton, J. M.; Geller, L. E.; Pechet, M. M. J. Am. Chem. Soc. 1961, 83, 4076. https://doi.org/10.1021/ja01480a030
  5. Sakamoto, T.; Kikugawa, Y. Synthesis 1993, 563.
  6. Corsaro, A.; Chiacchia, U.; Pistara, V. Synthesis 2001, 1903.
  7. Corsaro, A.; Chiacchio, M. A.; Pistarà, V. Current Organic Chemistry 2008, 482.
  8. Sahu, S.; Sahu, S.; Patel, S.; Dash, S.; Mishra, B. K. Indian Journal of Chemistry 2008, 47B, 259.
  9. Barhate, N. B.; Gajare, A. S.; Wakharkar, R. D.; Sudalai, A. Tetrahedron Lett. 1997, 38, 653. https://doi.org/10.1016/S0040-4039(96)02384-2
  10. Rao, C. G.; Radhakrishna, A. S.; Singh, B. B.; Bhatnagar, S. P. Synthesis 1983, 808.
  11. Drabowicz, J. Synthesis 1980, 125.
  12. McKillop, A.; Hunt, J. D.; Naylor, R. D.; Taylor, E. C. J. Am. Chem. Soc. 1971, 93, 4918. https://doi.org/10.1021/ja00748a050
  13. Imanzadeh, G. H.; Hajipour, A. R.; Mallakpour, S. E. Synth. Commun. 2003, 33, 735. https://doi.org/10.1081/SCC-120016316
  14. Khazaei, A.; Manesh, A. A.; Ghasemi, A. H. Synthesis 2004, 2784.
  15. Zhou, X-T.; Yuan, Q-L.; Ji, H-B. Tetrahedron Lett. 2010, 51, 613. https://doi.org/10.1016/j.tetlet.2009.11.078
  16. Reddy, M. S.; Narender, N.; Rama Rao, K. Synth Commun. 2004, 43, 3881.
  17. Gogoi, P.; Hazarika, P.; Konwar, D. J. Org. Chem. 2005, 70, 1934. https://doi.org/10.1021/jo0480287
  18. de Lijser, H. J. P.; Fardoun, F. H.; Sawyer, J. R.; Quant, M. Org. Lett. 2002, 4, 2325. https://doi.org/10.1021/ol025978a
  19. Imanzadeh, G. H.; Zamanloo, M. R.; Eskandari, H.; Banaei, A. R. Bull. Korean Chem. Soc. 2006, 27, 119. https://doi.org/10.5012/bkcs.2006.27.1.119
  20. Yang, Y.; Zhang, D.; Wu, L.-Z.; Chen, B.; Zhang, L.-P.; Tung, C.- H. J. Org. Chem. 2004, 69, 4788. https://doi.org/10.1021/jo049895e
  21. Shirini, F.; Mamaghani, M.; Rahmanzadeh, A. Arkivoc. 2007, 34.
  22. Li, Z.; Ding, R.-B.; Xing, Y.-L.; Shi, S.-Y. Synth Commun. 2005, 35, 2520.
  23. Ghorbani-Choghamarani, A.; Shiri, L.; Zeinivand, J. Bull. Korean Chem. Soc. 2008, 29, 2496. https://doi.org/10.5012/bkcs.2008.29.12.2496
  24. Kim, B. R.; Lee, H-G.; Kim, E. J.; Lee, S.-G.; Yoon, Y.-J. J. Org. Chem. 2010, 75, 484. https://doi.org/10.1021/jo902356e
  25. Velusamy, S.; Punniyamurthy, T. Org. Lett. 2004, 6, 217. https://doi.org/10.1021/ol036166x
  26. Csanyi, L. J.; Jaky, K.; Dombi, G.; Evanics, F.; Dezso, G.; Kota, Z. Journal of Molecular Catalysis A: Chemical 2003, 195, 101. https://doi.org/10.1016/S1381-1169(02)00542-3
  27. Maeda, Y.; Kakiuchi, N.; Matsumura, S.; Nishimura, T.; Kawamura, T.; Uemura, S. J. Org. Chem. 2002, 67, 6718. https://doi.org/10.1021/jo025918i
  28. Kirihara, M.; Ochiai, Y.; Takizawa, S.; Takahata, H.; Nemoto, H. Chem. Commun. 1999, 1387.
  29. Kobayashi, H.; Yamanaka, I. Chem. Lett. 2007, 36, 114. https://doi.org/10.1246/cl.2007.114
  30. Dewan, A.; K akati, D. K.; Das, B. K. Indian Journal of Chemistry 2010, 49A, 39.
  31. Maeda, Y.; Kakiuchi, N.; Mastsumura, S.; Nishimura, T.; Uemura, S. Tetrahedron Lett. 2001, 42, 8877. https://doi.org/10.1016/S0040-4039(01)01949-9
  32. Kodama, S.; Ueta, Y.; Yoshida, J.; Nomoto, A.; Yano, S.; Ueshima, M.; Ogawa,A. Dalton Trans. 2009, 9708.
  33. Radosevich, A. T. Musich, C.; Toste, F. D. J. Am. Chem. Soc. 2005, 127, 1090. https://doi.org/10.1021/ja0433424
  34. Dewan, A.; Sarma, T.; Bora, U.; Kakati, D. K. Tetrahedron Lett. 2011, 52, 2563. https://doi.org/10.1016/j.tetlet.2011.03.044
  35. Narasimhulu, M.; Mahesh, K. C.; Reddy, T. S.; Rajesh, K.; Venkateswarlu Y. Tetrahedron Lett. 2006, 47, 4381. https://doi.org/10.1016/j.tetlet.2006.04.096

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