Factors Interfering with the Oppenauer Oxidation of Amino Alcohols1
RE Lutz, RH Jordan, WL Truett
Index: Lutz et al. Journal of the American Chemical Society, 1950 , vol. 72, p. 4085,4089
Full Text: HTML
Citation Number: 4
Abstract
In recent attempts3 we found that, like quinine, 4a several typical aliphatic 1, 2-amino alcohols did not undergo the Oppenauer oxidation with aluminum t-butoxide and benzophenone or cyclohexanone. However, aluminum isopropoxide reductions of the corresponding, aiid other, a-amino ketones have proceeded without difficulty in all cases tried except the a-(N-alkyl-ethano1amino)-ketones which are cyclic. 6 It follows that under ...
Related Articles:
[Hoefle, M. L.; Blouin, L. T.; Fleming, R. W.; Hastings, S.; Hinkley, J. M.; et al. Journal of Medicinal Chemistry, 1991 , vol. 34, # 1 p. 12 - 19]
[Hoefle, M. L.; Blouin, L. T.; Fleming, R. W.; Hastings, S.; Hinkley, J. M.; et al. Journal of Medicinal Chemistry, 1991 , vol. 34, # 1 p. 12 - 19]