Bulletin of the Korean Chemical Society

  • 제33권2호
  • /
  • Pages.379-380
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  • 2012
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Preparation of 2,2-Difluoro-1-arylethenylstannane as a Precursor of 1,1-Diaryl-2,2-difluoroethenes

  • Lee, Hyo-Young (Department of Chemistry and Medical Chemistry, Yonsei University) ;
  • Jeon, Jong-Hee (Department of Chemistry and Medical Chemistry, Yonsei University) ;
  • Jeon, Sung-Lan (Department of Chemistry and Medical Chemistry, Yonsei University) ;
  • Jeong, In-Howa (Department of Chemistry and Medical Chemistry, Yonsei University)
  • 투고 : 2011.10.11
  • 심사 : 2011.12.05
  • 발행 : 2012.02.20
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참고문헌

  1. Ichikawa, J.; Wada, W.; Okauchi, T.; Minami, T. J. Chem. Soc. Chem. Commun. 1997, 1537-1538.
  2. Herpin, T. F.; Motherwell, W. B.; Roberts, B. P.; Roland, S.; Weible, J. M. Tetrahedron 1997, 53, 15085-15100. https://doi.org/10.1016/S0040-4020(97)10007-2
  3. Ichikawa, J.; Miyazaki, H.; Sakoda, K.; Wada, Y. J. Fluorine Chem. 2004, 125, 585-593. https://doi.org/10.1016/j.jfluchem.2004.01.004
  4. Moore, W. R.; Schatzman, G. L.; Jarvi, E. T.; Gross, R. S.; McCarthy, J. R. J. Am. Chem. Soc. 1992, 114, 360-361. https://doi.org/10.1021/ja00027a056
  5. Motherwell, W. B.; Tozer, M. J.; Ross, B. C. J. Chem. Soc. Chem. Commun. 1989, 1437-1439.
  6. Tozer, M. J.; Herpin, T. F.; Tetrahedron 1996, 52, 8619-8683. https://doi.org/10.1016/0040-4020(96)00311-0
  7. Percy, J. M. Contemp. Org. Synth. 1995, 2, 251-268. https://doi.org/10.1039/co9950200251
  8. Obayashi, M.; Ito, E.; Matsui, K.; Kondo, K. Tetrahedron Lett. 1982, 23, 2323-2326. https://doi.org/10.1016/S0040-4039(00)87332-3
  9. Edwards, M. L.; Stemerick, D. M.; Jarvi, E. T.; Matthews, D. P.; McCarthy, J. R. Tetrahedron Lett. 1990, 31, 5571-5574. https://doi.org/10.1016/S0040-4039(00)97899-7
  10. Piettre, S. R.; Cabanas, L. Tetrahedron Lett. 1996, 37, 5881-5884. https://doi.org/10.1016/0040-4039(96)01267-1
  11. Nowak, I.; Robins, M. J. Org. Lett. 2005, 7, 721-724. https://doi.org/10.1021/ol047416s
  12. Burton, D. J.; Yang, Z. -Y.; Morken, P. A. Tetrahedron 1994, 50, 2993-3063. https://doi.org/10.1016/S0040-4020(01)81105-4
  13. Ichikawa, J. J. Fluorine. Chem. 2000, 105, 257-263. https://doi.org/10.1016/S0022-1139(99)00268-7
  14. Raghavanpillai, A.; Burton, D. J. J. Org. Chem. 2006, 71, 194-201. https://doi.org/10.1021/jo051842p
  15. Ichikawa, J.; Fukui, H.; Ishibashi, Y. J. Org. Chem. 2003, 68, 7800-7804. https://doi.org/10.1021/jo034718j
  16. Bennett, A. J.; Percy, J. M.; Rock, M. H. Synlett 1992, 483-484.
  17. Howarth, J. A.; Owton, W. M.; Percy, J. M.; Rock, M. H. Tetrahedron 1995, 51, 10289-10302. https://doi.org/10.1016/0040-4020(95)00588-Y
  18. DeBoos, G. A.; Fullbrook, J. J.; Percy, J. M. Org. Lett. 2001, 3, 2859-2861. https://doi.org/10.1021/ol010135p
  19. Garayt, M. R.; Percy, J. M. Tetrahedron Lett. 2001, 42, 6377-6380. https://doi.org/10.1016/S0040-4039(01)01220-5
  20. Xue, L.; Lu, L.; Pedersen S. D.; Liu, Q.; Narske, R. M.; Burton, D. J. J. Org. Chem. 1997, 62, 1064-1071. https://doi.org/10.1021/jo9618785
  21. Burton, D. J.; Jairaj, V. J. Fluorine Chem. 2005, 126, 797-801. https://doi.org/10.1016/j.jfluchem.2005.02.015
  22. Choi, J. H.; Jeong, I. H. Tetrahedron Lett. 2008, 49, 952-955. https://doi.org/10.1016/j.tetlet.2007.12.028
  23. Choi, J. H.; Paul, K.; Jung, Y. H.; Jeong, I. H. Bull. Korean Chem. Soc. 2010, 31, 25. https://doi.org/10.5012/bkcs.2010.31.01.025
  24. Han, S. Y.; Choi, J. H.; Hwang, J. H.; Jeong, I. H. Bull. Korean Chem. Soc. 2010, 31, 1121-1122. https://doi.org/10.5012/bkcs.2010.31.5.1121
  25. Han, S. Y.; Jeong, I. H. Org. Lett. 2010, 12, 5518-5521. https://doi.org/10.1021/ol1024037

피인용 문헌

  1. Cross-Coupling Reactions of Double or Triple Electrophilic Templates for Alkene Synthesis vol.53, pp.2, 2012, https://doi.org/10.1055/s-0040-1707270