Bulletin of the Korean Chemical Society

  • 제27권1호
  • /
  • Pages.121-122
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  • 2006
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Selective Reduction of Aromatic Nitriles to Aldehydes by Lithium Diisobutylpiperidinohydroaluminate (LDBPA)

  • Ha, Ji-Hyun (Department of Chemistry, Kangwon National University) ;
  • Ahn, Jin-Hee (Medicinal Science Division, Korea Research Institute of Chemical Technology) ;
  • An, Duk-Keun (Department of Chemistry, Kangwon National University)
  • 발행 : 2006.01.20
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참고문헌

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  7. Organosilicon hydride: Fry, J. L. Chem. Comm. 1974, 45. Fry, J. L.; Ott, R. A. J. Org. Chem. 1981, 46, 602 https://doi.org/10.1021/jo00316a023
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  10. Lithium tris(dihexylamino)-aluminium hydride: Cha, J. S. Bull. Korean Chem. Soc. 1992, 13, 670
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  20. Cha, J. S.; Kwon, O. O.; Jeoung, M. K.; Kim, E. J. Bull Korean Chem. Soc. 1994, 15, 1021
  21. N,N'- Dimethylethylenediaminoaluminium hydride: Cha, J. S.; Jang, S. H.; Kwon, S. Y. Bull. Korean Chem. Soc. 2002, 23, 1697 https://doi.org/10.5012/bkcs.2002.23.12.1697
  22. Catecholalane : Cha, J. S.; Chang, S. W.; Kwon, O. O.; Kim, J. M. Synlett 1996, 165
  23. 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

피인용 문헌

  1. Application of Flow Chemistry to the Selective Reduction of Esters to Aldehydes vol.2012, pp.2, 2012, https://doi.org/10.1002/ejoc.201101458
  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. Reduction of aromatic nitriles into aldehydes using calcium hypophosphite and a nickel precursor vol.16, pp.35, 2018, https://doi.org/10.1039/C8OB01751D
  5. Selective Reduction of Aromatic Nitriles to Aldehydes by Lithium Diisobutylpiperidinohydroaluminate (LDBPA). vol.37, pp.21, 2006, https://doi.org/10.1002/chin.200621044
  6. New Synthetic Method of Aldehydes from Tertiary Amides by Lithium Diisobutylpiperidinohydroaluminate (LDBPA) vol.27, pp.11, 2006, https://doi.org/10.5012/bkcs.2006.27.11.1913
  7. Chemoselective Reduction of Esters to Aldehydes by Potassium Diisobutyl-t-butoxyaluminum Hydride (PDBBA) vol.28, pp.12, 2006, https://doi.org/10.5012/bkcs.2007.28.12.2517
  8. Partial and Chemoselective Reduction of Nitriles with Metal Diisobutyl-t-butoxyaluminum Hydrides vol.29, pp.11, 2006, https://doi.org/10.5012/bkcs.2008.29.11.2303
  9. 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
  10. Silver‐Sulphur Oxido‐Vanadium Cluster: A Newly Born Catalyst for Direct Reduction of Aryl Carboxylic Acids to Aldehydes via Mars and van Krevelen Mechanism vol.1, pp.13, 2006, https://doi.org/10.1002/slct.201600933
  11. Controlled Reduction of Tertiary Amides to the Corresponding Alcohols, Aldehydes, or Amines Using Dialkylboranes and Aminoborohydride Reagents vol.81, pp.9, 2006, https://doi.org/10.1021/acs.joc.6b00276
  12. Methods of Nitriles Synthesis from Amines through Oxidative Dehydrogenation vol.362, pp.19, 2020, https://doi.org/10.1002/adsc.202000635
  13. Recent developments in dehydration of primary amides to nitriles vol.7, pp.22, 2020, https://doi.org/10.1039/d0qo00843e