Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Reducing Characteristics of Metal Diisobutyl-t-butoxyaluminum Hydrides for Tertiary Amides

  • Choi, Seong-Jib (Department of Chemistry and Institute for Molecular Science and Fusion Technology, Kangwon National University) ;
  • Lee, Kang-Jin (Department of Chemistry and Institute for Molecular Science and Fusion Technology, Kangwon National University) ;
  • Lee, Gwi-Bin (Department of Chemistry and Institute for Molecular Science and Fusion Technology, Kangwon National University) ;
  • An, Duk-Keun (Department of Chemistry and Institute for Molecular Science and Fusion Technology, Kangwon National University)
  • Published : 2008.07.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Lithium aluminium hydride: Hudlicky, M. Reductions in Organic Chemistry; Ellis Horwood Limited: Chichester, England, 1984
  2. Sodium alumininohydrate: Zakharkin, L. I.; Maslin, D. N.; Gavrilenko, V. V. Tetrahedron 1969, 25, 5555 https://doi.org/10.1016/S0040-4020(01)83061-1
  3. Lithium dior triethoxyaluminohydride: Brown, H. C.; Tsukamoto, T. J. Am. Chem. Soc. 1964, 86, 1089 https://doi.org/10.1021/ja01060a025
  4. Aminoaluminum hydride: Muraki, M.; Mukaiyama, T. Chem. Lett. 1975, 875
  5. Sodium diethyldihydroaluminate (SDDA): Yoon, N. M.; Gyoung, Y. S. Bull. Korean Chem. Soc. 1992, 13, 341
  6. Diisobutylaluminum hydride: Zakharkin, L. I.; Khorlina, I. M. Dokl. Akad. Nauk SSSR 1959, 2146
  7. Lithium diisobutylpiperidinohydroaluminate: Woo, S. M.; Kim, M. E.; An, D. K. Bull. Korean Chem. Soc. 2006, 27, 121 https://doi.org/10.5012/bkcs.2006.27.11.1913
  8. Kim, M. S.; Choi, Y. M.; An, D. K. Tetrahedron Lett. 2007, 48, 5061 https://doi.org/10.1016/j.tetlet.2007.05.091
  9. Song, J. I.; An, D. K. Chem. Lett. 2007, 36, 886 https://doi.org/10.1246/cl.2007.886
  10. Chae, M. J.; Song, J. I.; An, D. K. Bull. Korean Chem. Soc. 2007, 28, 2517 https://doi.org/10.5012/bkcs.2007.28.12.2517

Cited by

  1. A novel method for the one-pot conversion of carboxylic acids to N,N-dimethylamides vol.9, pp.6, 2012, https://doi.org/10.1007/s13738-012-0112-5
  2. -Butoxyaluminum Hydride (LDBBA) vol.36, pp.12, 2015, https://doi.org/10.1002/bkcs.10571
  3. Synthesis of Aldehydes from Tertiary Amides Using a Novel Modified Red-Al Reducing Agent vol.36, pp.7, 2015, https://doi.org/10.1002/bkcs.10352
  4. : Evolution of Synthetic Strategies to a Streamlined Process vol.22, pp.25, 2016, https://doi.org/10.1002/chem.201601449
  5. ChemInform Abstract: Reducing Characteristics of Metal Diisobutyl-t-butoxyaluminum Hydrides for Tertiary Amides. vol.39, pp.47, 2008, https://doi.org/10.1002/chin.200847048
  6. Lithium Diisobutylmorpholinoaluminum Hydride (LDBMOA) as an Effective Partial Reducing Agent for Tertiary Amides and Nitriles vol.33, pp.12, 2012, https://doi.org/10.5012/bkcs.2012.33.12.4194
  7. Controlled Reduction of Tertiary Amides to the Corresponding Alcohols, Aldehydes, or Amines Using Dialkylboranes and Aminoborohydride Reagents vol.81, pp.9, 2008, https://doi.org/10.1021/acs.joc.6b00276
  8. Alkene hydroboration with pinacolborane catalysed by lithium diisobutyl-tert-butoxyaluminum hydride vol.9, pp.45, 2008, https://doi.org/10.1039/c9ra04699b