Sodium borohydride in carboxylic acid media: A phenomenal reduction system

Chemical Society Reviews

Volumn 27, Issue 6, 1998, Pages 395-404

  Gribble, Gordon W ^a  

^a Dartmouth College   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0032328845     PISSN: 03060012     EISSN: None     Source Type: Journal    
DOI: 10.1039/a827395z     Document Type: Article

References (7)

1. For a review and historical background on acyloxyborohydrides, see: G. W. Gribble and C. F. Nutaitis, Org. Prep. Proc. Int., 1985, 17, 317.
2. For recent reviews of the synthetic utility of acyloxyborohydrides, see: (a) G. W. Gribble, in Reductions in Organic Synthesis, ed. Ahmed F. Abdel-Magid, ACS Symposium Series 641, American Chemical Society, Washington, DC, 1996, pp. 167-200; (b) G. W. Gribble, Chemtech, 1996, 12, 26.
3. For recent reviews of the synthetic utility of acyloxyborohydrides, see: (a) G. W. Gribble, in Reductions in Organic Synthesis, ed. Ahmed F. Abdel-Magid, ACS Symposium Series 641, American Chemical Society, Washington, DC, 1996, pp. 167-200; (b) G. W. Gribble, Chemtech, 1996, 12, 26.
4. J. A. Marshall and W. S. Johnson, J. Org. Chem., 1963, 28, 421.
5. G. W. Gribble, P. D. Lord, J. Skotnicki, S. E. Dietz, J. T. Eaton and J. L. Johnson, J. Am. Chem. Soc., 1974, 96, 7812.
6. G. W. Gribble and J. H. Hoffman, Synthesis, 1977, 859.
7. M. Somei, F. Yamada and H. Morikawa, Heterocycles, 1997, 46, 91.