Bulletin of the Korean Chemical Society

  • 제15권11호
  • /
  • Pages.1021-1023
  • /
  • 1994
  • /
  • 0253-2964(pISSN)
  • /
  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
권호 표지
DOI QR코드

DOI QR Code

Conversion of Nitriles into Aldehydes by Diisobutylaluminum Hydride-Dimethyl Sulfide Complex

  • 발행 : 1994.11.20
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

키워드

참고문헌

  1. J. Chem. Soc. v.127 Stephen, E.
  2. Angew. Chem. v.68 Sodium triethoxyaluminohydride Hesse, G.;Schrodel, R.
  3. Ann. v.607 Sodium Triethoxyaluminohydride Hesse, G.;Schrodel, R.
  4. Tetrahedron Lett. Lithium triethoxyaluminohydride Brown, H. C.;Schoaf, C. J.;Garg, C. P.
  5. J. Chem. Educ. v.38 Brown, H. C.
  6. J. Am. Chem. Soc. v.86 Brown, H. C.;Garg, C. P.
  7. Bull. Soc. Chim. Fr. de Peretti, D.;Strzalko-Bottin, T.;Seydenpenne, J.
  8. Dokl. Akad. Nauk SSSR v.116 Diisobutylaluminum hydride Zakharkin, L. I.;Khorlina, I. M.
  9. J. Chem. Soc. [c] Minato, H.;Nagasaki, T.
  10. Rec. Trav. Chim. Pays-Bas v.85 Haeck, H. H.;Kralt, T.
  11. J. Org. Chem. v.24 Miller, A. E. G.;Bliss, J. W.;Schwartzman, L. H.
  12. Recherches v.14 Teisseire, P.;Plattier, M.;Corbier, B.
  13. J. Org. Chem. v.35 Marshall, J. A.;Andersen, N. H.;Johnson, P. C.
  14. J. Org. Chem. v.37 Stevens, R. V.;Dupree, Jr., L. E.;Loewenstein, P. L.
  15. Tetrahedron Lett. Caton, M. P. L.;Coffee, E. C. J.;Watkins, G. L.
  16. Bull. Korean Chem. Soc. v.7 Yoon, N. M.;Kim, S. K.;Gyong, Y. S.
  17. Gazz. Chim. Ital. v.85 Peitra, S.;Trinchera, C.
  18. Compt. Rend. v.252 Gaiffe, A.;Pallaud, R.
  19. Compt. Rend. v.254 Gaiffe, A.;Pallaud, R.
  20. Angew. Chem. v.67 Plieninger, H.;Werst, G.
  21. Chem. Ber. v.88 Plieninger, H.;Werst, G.
  22. J. Org. Chem. v.27 Coker, J. N.;Kohlhase, W. L.;Fields, M.;Rogers, A. O.;Stevens, M. A.
  23. J. Chem. Soc. Staskun, B.;Backeberg, O. G.
  24. J. Chem. Soc. van Es, T.;Staskun, B.
  25. Org. Syn. v.51 van Es, T.;Staskun, B.
  26. Chem. Comm. Fry, J. L.
  27. J. Org. Chem. v.46 Fry, J. L.;Ott, R. A.
  28. Bull. Korean Chem. Soc. v.8 Cha, J. S.;Oh, S. Y.;Kim, J. E.
  29. Tetrahedron Lett. v.30 Cha, J. S.;Yoon, M. S.
  30. Org. Prep. Proced. Int. v.24 Cha, J. S.;Lee, S. E.;Lee, H. S.
  31. Bull. Korean Chem. Soc. v.13 Cha, J. S.
  32. Org. Prep. Proced. Int. v.26 Cha, J. S.;Jeoung, M. K.;Kim, J. M.;Kwon, O. O.;Lee, J. C.
  33. Bull. Korean Chem. Soc. v.15 Cha, J. S.;Jeoung, M. K.;Kwon, O. O.;Lee, K. D.;Lee, H. S.
  34. J. Org. Chem. v.50 Yoon, N. M.;Gyoung, Y. S.
  35. CRC Handbook of Tables for Organic Compound Identification

피인용 문헌

  1. ChemInform Abstract: Conversion of Nitriles into Aldehydes by Diisobutylaluminum Hydride- Dimethyl Sulfide Complex. vol.26, pp.32, 1994, https://doi.org/10.1002/chin.199532088
  2. Selective Conversion of Aromatic Nitriles to Aldehydes by Lithium N,N'-Dimethylethylenediaminoaluminum Hydride vol.23, pp.12, 1994, https://doi.org/10.5012/bkcs.2002.23.12.1697
  3. Selective Reduction of Aromatic Nitriles to Aldehydes by Lithium Diisobutylpiperidinohydroaluminate (LDBPA) vol.27, pp.1, 1994, https://doi.org/10.5012/bkcs.2006.27.1.121
  4. Partial and Chemoselective Reduction of Nitriles with Metal Diisobutyl-t-butoxyaluminum Hydrides vol.29, pp.11, 1994, https://doi.org/10.5012/bkcs.2008.29.11.2303
  5. A New Method of Partial and Chemoselective Reduction of Nitriles to Aldehydes by Lithium Diisobutyl-iso-propoxyaluminum Hydride (LDBIPA) vol.31, pp.2, 1994, https://doi.org/10.5012/bkcs.2010.31.02.473
  6. Thirty Six Years of Research on the Selective Reduction and Hydroboration vol.32, pp.6, 1994, https://doi.org/10.5012/bkcs.2011.32.6.1808
  7. Some Recommended Procedures for Conversion of Carboxylic Acid and Its Derivatives to Aldehydes by Metal Hydride Reductions vol.5, pp.2, 2012, https://doi.org/10.13160/ricns.2012.5.2.084
  8. Pentafulvene for the Synthesis of Complex Natural Products: Total Syntheses of (±)‐Pallambins A and B vol.127, pp.38, 1994, https://doi.org/10.1002/ange.201505126
  9. Pentafulvene for the Synthesis of Complex Natural Products: Total Syntheses of (±)‐Pallambins A and B vol.54, pp.38, 1994, https://doi.org/10.1002/anie.201505126
  10. Largazole Analogues Embodying Radical Changes in the Depsipeptide Ring: Development of a More Selective and Highly Potent Analogue vol.59, pp.23, 1994, https://doi.org/10.1021/acs.jmedchem.6b01271