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One-Pot Synthesis of Alkyl Aryl Selenides with Hydroxy-, Amino-, and Carboxy-Functionality from Aryl Halides

  • Chin, Jung-Wook (Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Sciences, Seoul National University) ;
  • Tak, Jun-Gae (Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Sciences, Seoul National University) ;
  • Hahn, Dong-Yup (Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Sciences, Seoul National University) ;
  • Yang, In-Ho (Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Sciences, Seoul National University) ;
  • Ko, Jae-Young (Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Sciences, Seoul National University) ;
  • Ham, Jung-Yeob (Korea Institute of Science and Technology, Gangneung Institute) ;
  • Kang, Heon-Joong (Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Sciences, Seoul National University)
  • Published : 2009.02.20

Abstract

Keywords

References

  1. Mugesh, G.; du Mont, W.-W.; Sies, H. Chem. Rev. 2001, 101, 2125. https://doi.org/10.1021/cr000426w
  2. Nogueira, C. W.; Zeni, G.; Rocha, J. B. T. Chem. Rev. 2004, 104, 6255. https://doi.org/10.1021/cr0406559
  3. Schrauzer, G. N. Cell. Mol. Life Sci. 2000, 57, 1864. https://doi.org/10.1007/PL00000668
  4. Sinha, R.; El-Bayoumy, K. Curr. Cancer Drug Targets 2004, 4, 13. https://doi.org/10.2174/1568009043481614
  5. El-Bayoumy, K.; Rao, C. V.; Reddy, B. S. Nutr. Cancer 2001, 40, 18. https://doi.org/10.1207/S15327914NC401_6
  6. Ham, J.; Yang, I.; Kang, H. J. Org. Chem. 2004, 69, 3236. https://doi.org/10.1021/jo049758h
  7. Ham, J.; Kang, H. Tetrahedron Lett. 2005, 46, 6683. https://doi.org/10.1016/j.tetlet.2005.07.145
  8. Ham, J.;Cho, S. J.; Ko, J.; Chin, J.; Kang, H. J. Org. Chem. 2006, 71, 5781. https://doi.org/10.1021/jo060361i
  9. Ko, J.; Ham, J.; Yang, I.; Chin, J.; Nam, S.-J.; Kang, H. Tetrahedron Lett. 2006, 47, 7101. https://doi.org/10.1016/j.tetlet.2006.07.056
  10. Patai, S.; Rappoport, Z. In The Chemistry of Organic Selenium and Tellurium Compounds; Wiley & Sons: New York, 1986 and 1987; Vol. 1 and 2.

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