Tham khảo Liti_nhôm_hydrua

  1. ↑ Finholt, A. E.; Bond, A. C.; Schlesinger, H. I. (1947). “Lithium Aluminum Hydride, Aluminum Hydride and Lithium Gallium Hydride, and Some of their Applications in Organic and Inorganic Chemistry”. Journal of the American Chemical Society. 69 (5): 1199–1203. doi:10.1021/ja01197a061.
  2. 1 2 3 Gerrans, G. C.; Hartmann-Petersen, P. (2007). “Lithium Aluminium Hydride”. Sasol Encyclopaedia of Science and Technology. New Africa Books. tr. 143. ISBN 1-86928-384-8.
  3. ↑ Keese, R.; Brändle, M.; Toube, T. P. (2006). Practical Organic Synthesis: A Student's Guide. John Wiley and Sons. tr. 134. ISBN 0-470-02966-8.
  4. ↑ Andreasen, A.; Vegge, T.; Pedersen, A. S. (2005). “Dehydrogenation Kinetics of as-Received and Ball-Milled LiAlH4” (PDF). Journal of Solid State Chemistry. 178 (12): 3672–3678. Bibcode:2005JSSCh.178.3672A. doi:10.1016/j.jssc.2005.09.027. Bản gốc (PDF) lưu trữ ngày 3 tháng 3 năm 2016. Truy cập ngày 30 tháng 9 năm 2017.
  5. ↑ Pohanish, R. P. (2008). Sittig's Handbook of Toxic and Hazardous Chemicals and Carcinogens (ấn bản 5). William Andrew Publishing. tr. 1540. ISBN 978-0-8155-1553-1.
  6. ↑ Brown, H. C. (1951). “Reductions by Lithium Aluminum Hydride”. Organic Reactions. 6: 469. doi:10.1002/0471264180.or006.10. ISBN 0471264180.
  7. ↑ Seebach, D.; Kalinowski, H.-O.; Langer, W.; Crass, G.; Wilka, E.-M. (1991). “Chiral Media for Asymmetric Solvent Inductions. (S,S)-(+)-1,4-bis(Dimethylamino)-2,3-Dimethoxybutane from (R,R)-(+)-Diethyl Tartrate”. Organic Syntheses.; Collective Volume, 7, tr. 41
  8. ↑ Park, C. H.; Simmons, H. E. (1974). “Macrocyclic Diimines: 1,10-Diazacyclooctadecane”. Organic Syntheses. 54: 88.; Collective Volume, 6, tr. 382
  9. ↑ Chen, Y. K.; Jeon, S.-J.; Walsh, P. J.; Nugent, W. A. (2005). “(2S)-(−)-3-exo-(Morpholino)Isoborneol”. Organic Syntheses. 82: 87.
  10. ↑ “Red-Al, Sodium bis(2-methoxyethoxy)aluminumhydride”. Organic Chemistry Portal.
  11. ↑ Reetz, M. T.; Drewes, M. W.; Schwickardi, R. (1999). “Preparation of Enantiomerically Pure α-N,N-Dibenzylamino Aldehydes: S-2-(N,N-Dibenzylamino)-3-Phenylpropanal”. Organic Syntheses. 76: 110.; Collective Volume, 10, tr. 256
  12. ↑ Oi, R.; Sharpless, K. B. (1996). “3-[(1S)-1,2-Dihydroxyethyl]-1,5-Dihydro-3H-2,4-Benzodioxepine”. Organic Syntheses. 73: 1.; Collective Volume, 9, tr. 251
  13. ↑ Koppenhoefer, B.; Schurig, V. (1988). “(R)-Alkyloxiranes of High Enantiomeric Purity from (S)-2-Chloroalkanoic Acids via (S)-2-Chloro-1-Alkanols: (R)-Methyloxirane”. Organic Syntheses. 66: 160.; Collective Volume, 8, tr. 434
  14. ↑ Barnier, J. P.; Champion, J.; Conia, J. M. (1981). “Cyclopropanecarboxaldehyde”. Organic Syntheses. 60: 25.; Collective Volume, 7, tr. 129
  15. ↑ Elphimoff-Felkin, I.; Sarda, P. (1977). “Reductive Cleavage of Allylic Alcohols, Ethers, or Acetates to Olefins: 3-Methylcyclohexene”. Organic Syntheses. 56: 101.; Collective Volume, 6, tr. 769
  16. ↑ Rickborn, B.; Quartucci, J. (1964). “Stereochemistry and Mechanism of Lithium Aluminum Hydride and Mixed Hydride Reduction of 4-t-Butylcyclohexene Oxide”. The Journal of Organic Chemistry. 29 (11): 3185–3188. doi:10.1021/jo01034a015.
  17. ↑ Wade, L. G. Jr. (2006). Organic Chemistry (ấn bản 6). Pearson Prentice Hall. ISBN 0-13-147871-0.
  18. ↑ Johnson, J. E.; Blizzard, R. H.; Carhart, H. W. (1948). “Hydrogenolysis of Alkyl Halides by Lithium Aluminum Hydride”. Journal of the American Chemical Society. 70 (11): 3664–3665. doi:10.1021/ja01191a035. PMID 18121883.
  19. ↑ Krishnamurthy, S.; Brown, H. C. (1982). “Selective Reductions. 28. The Fast Reaction of Lithium Aluminum Hydride with Alkyl Halides in THF. A Reappraisal of the Scope of the Reaction”. The Journal of Organic Chemistry. 47 (2): 276–280. doi:10.1021/jo00341a018.
  20. ↑ Carruthers, W. (2004). Some Modern Methods of Organic Synthesis. Cambridge University Press. tr. 470. ISBN 0-521-31117-9.
  21. ↑ Wender, P. A.; Holt, D. A.; Sieburth, S. Mc N. (1986). “2-Alkenyl Carbinols from 2-Halo Ketones: 2-E-Propenylcyclohexanol”. Organic Syntheses. 64: 10.; Collective Volume, 7, tr. 456

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