Lithium Diisobutyl-n-butylaluminum Hydride. An Exceptionally Powerful and Selective Reducing Agent in Reduction of Organic Halides

References

1. Synthesis A. R. Pinder
2. J. Org. Chem. v.43 E. C. Ashby;J. J. Lin
3. J. Org. Chem. v.45 S. Krishnamurthy;H. C. Brown
4. Tetrahedron v.37 H. Toi;Y. Yamamoto;A. Sonoda;S-I. Murahashi
5. J. Org. Chem. v.46 R. Vanderesse;J-J. Brunet;P. Caubere
6. J. Org. Chem. v.47 S. Krishnamurthy;H. C. Brown
7. J. Amer. Chem. Soc. v.89 G. Zweifel;R. Steele
8. Izv. Akad. Nauk. USSR, Ser Khim. v.11 L. I. Zakharkin;N. V. Grandberg
9. Chem. Abstr. v.86 L. I. Zakharkin;N. V. Grandberg
10. Synthesis G. Kovacs;G. Galambos;Z. Juvancz
11. J. Org. Chem. v.45 B. M. Trostand;G. T. Rivers;M. Gold
12. J. Org. Chem. v.36 R. O. Hutchins;R. J. Bertsch;D. Hoke
13. J. Amer. Chem. Soc. v.102 B. M. Trost;L.N. Jungheim
14. J. Org. Chem. v.47 Kim, S. K.;H. Ahn;Y. W. Chung
15. J. Amer. Chem. Soc. v.99 H. C. Brown;A. Khuri;S. Krishnamurthy
16. J. Amer. Chem. Soc. v.99 S. J. Krishnamurthy
17. J. Org. Chem. v.45 S. Krishnamurthy
18. J. Amer. Chem. Soc. v.94 C. W. Jefford;D. Kirkpatrick;F. Delay
19. Tetrahedron C. W. Jefford;U. Burger
20. J. Amer. Chem. Soc. v.85 H. C. Brown;S. Krishnamurthy
21. J. Amer. Chem. Soc. v.95 S. Masamune;P. A. Rossy;G. S. Bates
22. J. Amer. Chem. Soc. v.96 S. masamune;G. S. P. Bates;E. Georghiou
23. Chem. Soc. Chem. Commun. v.762 T. Yoshida;E. J. Negishi
24. J. Org. Chem. v.42 R. O. Hutchins;D. Kandasamy;C. A. Maryanoff;D. Masilamani;B. E. Maryanoff