Bulletin of the Korean Chemical Society

  • 제30권2호
  • /
  • Pages.496-498
  • /
  • 2009
  • /
  • 0253-2964(pISSN)
  • /
  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
권호 표지
DOI QR코드

DOI QR Code

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)
  • 발행 : 2009.02.20
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

키워드

참고문헌

  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.

피인용 문헌

  1. Synthesis of an Urea-substituted Selenoisobutyric Acid Isostere of the Peroxisome Proliferator-activated Receptor α Selective Agonist vol.32, pp.11, 2011, https://doi.org/10.5012/bkcs.2011.32.11.4089
  2. Regioselective Synthesis of Selenide Ethers through a Decarboxylative Coupling Reaction vol.359, pp.22, 2017, https://doi.org/10.1002/adsc.201700676
  3. Microwave synthesis of bis(cycloalkeno)-1,4-diselenins: a novel source of Se for CdSe QDs vol.41, pp.15, 2017, https://doi.org/10.1039/C7NJ00793K
  4. ChemInform Abstract: One-Pot Synthesis of Alkyl Aryl Selenides with Hydroxy-, Amino-, and Carboxy-Functionality from Aryl Halides. vol.40, pp.28, 2009, https://doi.org/10.1002/chin.200928159
  5. Silicon-Assisted Synthesis and Functionalization of Sulfurated and Selenated Compounds vol.190, pp.8, 2015, https://doi.org/10.1080/10426507.2015.1024790
  6. Bis(trimethylsilyl)selenide in the Selective Synthesis of β‐Hydroxy, β‐Mercapto, and β‐Amino Diorganyl Diselenides and Selenides Through Ring Opening of Strained Heter vol.2015, pp.2, 2009, https://doi.org/10.1002/ejoc.201403015