Diastereoselective reduction of acyclic N-aryl-β-amino ketones
Abstract
A stereoselective route to anti- and syn-N-aryl-γ-amino alcohols is reported featuring the reduction of the corresponding β-amino ketones with Et3BHLi or Zn(BH4)2, respectively.
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J. Chem. Soc., Perkin Trans. 1, 1990, 1213-1214
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Diastereoselective reduction of acyclic N-aryl-β-amino ketones
R. A. Pilli, D. Russowsky and L. C. Dias, J. Chem. Soc., Perkin Trans. 1, 1990, 1213 DOI: 10.1039/P19900001213
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