Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Synthesis of 2,3,4-Trisubstituted 2,5-Dihydrofuran Derivatives

  • Gowrisankar, Saravanan (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Park, Da-Yeon (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Kim, Jae-Nyoung (Department of Chemistry and Institute of Basic Science, Chonnam National University)
  • Published : 2005.11.20
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References

  1. Nakamura, M.; Liang, C.; Nakamura, E. Org. Lett. 2004, 6, 2015 https://doi.org/10.1021/ol0493554
  2. Bottex, M.; Cavicchioli, M.; Hartmann, B.; Monteiro, N.; Balme, G. J. Org. Chem. 2001, 66, 175 https://doi.org/10.1021/jo0012997
  3. Marat, X.; Monteiro, N.; Balme, G Synlett 1997, 845
  4. Monteiro, N.; Balme, G. J. Org. Chem. 2000, 65, 3223 https://doi.org/10.1021/jo991817h
  5. Azoulay, S.; Monteiro, N.; Balme, G. Tetrahedron Lett. 2002, 43, 9311 https://doi.org/10.1016/S0040-4039(02)02383-3
  6. Roy, S. C.; Guin, C.; Rana, K. K.; Maiti, G. Tetrahedron 2002, 58, 2435 https://doi.org/10.1016/S0040-4020(02)00113-8
  7. Maiti, G.; Adhikari, S.; Roy, S. C. Tetrahedron 1995, 51, 8389 https://doi.org/10.1016/0040-4020(95)00450-M
  8. Adhikari, S.; Roy, S. C. Tetrahedron Lett. 1992, 33, 6025 https://doi.org/10.1016/S0040-4039(00)61118-8
  9. Roy, S. C.; Adhikari, S. Tetrahedron 1993, 49, 8415 https://doi.org/10.1016/S0040-4020(01)81924-4
  10. Clique, B.; Monteiro, N.; Balme, G. Tetrahedron Lett. 1999, 40, 1301 https://doi.org/10.1016/S0040-4039(98)02631-8
  11. Woods, M.; Monteiro, N.; Balme, G. Eur. J. Org. Chem. 2000, 1711
  12. Hojo, M.; Ishibashi, N.; Hosomi, A. Synlett 1996, 234
  13. Ma, S.; Gao, W. J. Org. Chem. 2002, 67, 6104 https://doi.org/10.1021/jo0163997
  14. Dunach, E.; Esteves, A. P.; Medeiros, M. J.; Olivero, S. Tetrahedron Lett. 2004, 45, 7935 https://doi.org/10.1016/j.tetlet.2004.08.131
  15. Esteves, A. P.; Goken, D. M.; Klein, L. J.; Lemos, M. A.; Medeiros, M. J.; Peters, D. G. J. Org. Chem. 2003, 68, 1024 https://doi.org/10.1021/jo026102k
  16. Maiti, G.; Adhikari, S.; Roy, S. C. J. Chem. Soc., Perkin Trans. 1 1995, 927
  17. Yang, C.; Murray, W. V.; Wilson, L. J. Tetrahedron Lett. 2003, 44, 1783 https://doi.org/10.1016/S0040-4039(03)00083-2
  18. Marco, J. A.; Carda, M.; Rodriguez, S.; Castillo, E.; Kneeteman, M. N. Tetrahedron 2003, 59, 4085 https://doi.org/10.1016/S0040-4020(03)00584-2
  19. Ma, S.; Zhang, J. J. Am. Chem. Soc. 2003, 125, 12386 https://doi.org/10.1021/ja036616g
  20. Garcon, S.; Vassiliou, S.; Cavicchioli, M.; Hartmann, B.; Monteiro, N.; Balme, G. J. Org. Chem. 2001, 66, 4069 https://doi.org/10.1021/jo0017990
  21. Lee, Y. R.; Kim, N. S.; Kim, B. S. Tetrahedron Lett. 1997, 38, 5671 https://doi.org/10.1016/S0040-4039(97)01235-5
  22. Wenkert, E.; Khatuya, H.; Klein, P. S. Tetrahedron Lett. 1999, 40, 5171 https://doi.org/10.1016/S0040-4039(99)01007-2
  23. Ohe, K.; Matsuda, H.; Morimoto, T.; Ogoshi, S.; Chatani, N.; Murai, S. J. Am. Chem. Soc. 1994, 116, 4125 https://doi.org/10.1021/ja00088a077
  24. Gowrisankar, S.; Lee, K. Y.; Kim, J. N. Tetrahedron Lett. 2005, 46, 4859 https://doi.org/10.1016/j.tetlet.2005.05.057
  25. Jana, S.; Guin, C.; Roy, S. C. Tetrahedron Lett. 2005, 46, 1155 https://doi.org/10.1016/j.tetlet.2004.12.079

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