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Chemoselective Reduction of Esters to Aldehydes by Potassium Diisobutyl-t-butoxyaluminum Hydride (PDBBA)

  • Chae, Min-Jung (Department of Chemistry, Kangwon National University) ;
  • Song, Jung-In (Department of Chemistry, Kangwon National University) ;
  • An, Duk-Keun (Department of Chemistry, Kangwon National University)
  • Published : 2007.12.20
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References

  1. Zakharkin, L. I.; Khorlina, I. M. Tetrahedron Lett. 1962, 619
  2. Weissman, P. M.; Brown, H. C. J. Org. Chem. 1966, 31, 283 https://doi.org/10.1021/jo01339a063
  3. Muraki, M.; Mukaiyama, T. Chem. Lett. 1975, 215
  4. Yoon, N. M.; Ahn, J. H.; An, D. K.; Shon, Y. S. J. Org. Chem. 1993, 58, 1941 https://doi.org/10.1021/jo00059a058
  5. Yoon, N. M.; Shon, Y. S.; Ahn, J. H.; An, J. W. Bull. Korean Chem. Soc. 1993, 14, 522
  6. Ahn, J. H.; Song, J. I.; Ahn, J. E.; An, D. K. Bull. Korean Chem. Soc. 2005, 26, 377 https://doi.org/10.1007/s11814-009-0063-4
  7. Ha, J. H.; Ahn, J. H.; An, D. K. Bull. Korean Chem. Soc. 2006, 27, 121 https://doi.org/10.5012/bkcs.2006.27.1.121
  8. Woo, S. M.; Kim, M. E.; An, D. K. Bull. Korean Chem. Soc. 2006, 27, 1913 https://doi.org/10.5012/bkcs.2006.27.11.1913
  9. Kim, M. S.; Choi, Y. M.; An, D. K. Tetrahedron Lett. 2007, 48, 5061 https://doi.org/10.1016/j.tetlet.2007.05.091
  10. Song, J. I.; An, D. K. Chem. Lett. 2007, 36, 886 https://doi.org/10.1246/cl.2007.886

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