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Double Suzuki Reactions of Organoboronic Acids with 1,n-Dibromides


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References

  1. Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457. https://doi.org/10.1021/cr00039a007
  2. Suzuki, A. J. Organomet. Chem. 1999, 576, 147. https://doi.org/10.1016/S0022-328X(98)01055-9
  3. Cammidge, A. N.; Crepy, K. V. L. Chem. Commun. 2000,1723.
  4. Yin, J.; Buchwald, S. L. J. Am. Chem. Soc. 2000, 122,12051. https://doi.org/10.1021/ja005622z
  5. Hayashi, T.; Niizuma, S.; Kamikawa, T.; Suzuki, N.; Uozumi,Y. J. Am. Chem. Soc. 1995, 117, 9101. https://doi.org/10.1021/ja00140a041
  6. Kamikawa, T.; Hayashi,T. Tetrahedron 1999, 55, 3455. https://doi.org/10.1016/S0040-4020(98)01154-5
  7. Burk, M. J.; Allen, J. G.; Kiesman, W. F. J. Am. Chem. Soc.1998, 120, 657. https://doi.org/10.1021/ja9731074
  8. Henaff, N.; Whiting, A. J. Chem. Soc., PerkinTrans. 1 2000, 395.
  9. Roush, W. R.; Moriarty, K. J.; Brown, B. B. Tetrahedron Lett.1990, 31, 6509. https://doi.org/10.1016/S0040-4039(00)97103-X
  10. Uenishi, J.; Kawahama, R.; Yonemitsu, O.;Tsuji, J. J. Org. Chem. 1996, 61, 5716. https://doi.org/10.1021/jo961013r
  11. Roush, W. R.; Moriarty, K. J.; Brown, B. B. Tetrahedron Lett.1990, 31, 6509. https://doi.org/10.1016/S0040-4039(00)97103-X
  12. Roush, W. R.; Reilly, M. L.; Kayama, K.;Brown, B. B. J. Org. Chem. 1997, 62, 8708. https://doi.org/10.1021/jo970960c
  13. Baldwin, J. E.;Chesworth, R.; Paker, J. S.; Russell, A. T. Tetrahedron Lett. 1995,36, 9551. https://doi.org/10.1016/0040-4039(95)02045-4
  14. Shen, W. Synlett 2000, 737.
  15. Minato, A.; Suzuki, K. J. Am. Chem. Soc. 1987, 109, 1257. https://doi.org/10.1021/ja00238a052
  16. Minato, A. J. Org. Chem. 1991,56, 4052. https://doi.org/10.1021/jo00012a048
  17. Panek, J. S.; Hu, T. J. Org. Chem. 1997, 62, 4912. https://doi.org/10.1021/jo970647a
  18. Xu, C.; Negishi, E. Tetrahedron Lett. 1999, 40, 431. https://doi.org/10.1016/S0040-4039(98)02394-6
  19. Duan, Z.; Sun, W.-H.; Liu, Y.;Takahashi, T. Tetrahedron Lett. 2000, 41, 7471. https://doi.org/10.1016/S0040-4039(00)01277-6
  20. Wang,L.; Shen, W. Tetrahedron Lett. 1998, 39, 7625. https://doi.org/10.1016/S0040-4039(98)01690-6
  21. Uenishi, J.;Kawahama, R.; Yonemitsu, O.; Tsuji, J. J. Org. Chem. 1996, 61,5716. https://doi.org/10.1021/jo961013r
  22. Uenishi, J.; Matsui, K. Tetrahedron Lett. 2001, 42, 4353. https://doi.org/10.1016/S0040-4039(01)00749-3
  23. Ogasawara, M.; Ikeda, H.; Ohtsuki,K.; Hayashi, T. Chem. Lett. 2000, 776.
  24. Leimner, J.; Weyerstahl, P. Chem. Ber. 1982, 115, 3697. https://doi.org/10.1002/cber.19821151203
  25. Henaff, N.; Whiting, A. J. Chem. Soc., Perkin Trans. 1 2000, 395.
  26. Liu, Y.; Gribble, G. W. Tetrahedron Lett. 2000, 41, 8717. https://doi.org/10.1016/S0040-4039(00)01564-1
  27. Galda, P.; Rehahn, M. Synthesis 1996, 614.
  28. Brown, H. C.; Gupta, S. K. J. Am. Chem. Soc. 1975, 97, 5249. https://doi.org/10.1021/ja00851a038
  29. Brown, H. C.; Bhat, N. G.; Somayaji, V. Organometallics1983, 2, 1311. https://doi.org/10.1021/om50004a008
  30. Shen, W. Synlett 2000, 737.
  31. Liu, Y.; Gribble, G. W. Tetrahedron Lett. 2001, 41, 8717.
  32. Henaff, N.; Whiting, A. J. Chem. Soc., Perkin Trans. 1 2000, 395.
  33. Roush, W. R.; Moriarty, K. J.; Brown, B. B. Tetrahedron Lett.1990, 31, 6509. https://doi.org/10.1016/S0040-4039(00)97103-X
  34. Shen, W. Synlett 2000, 737.
  35. Smith, K. A.; Campi, E. M.; Jackson, W. R.; Marcuccio, S.;Naeslund, C. G. M.; Deacon, G. B. Synlett 1997, 131.

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