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Enzymes in organic synthesis. 32. Stereospecific horse liver alcohol dehydrogenase-catalyzed oxidations of exo - and endo -oxabicyclic meso diols

  • Jones J
  • Francis C
Canadian Journal of Chemistry (1984) 62(11) 2578-2582
DOI: 10.1139/v84-440
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Abstract

Preparative-scale horse liver alcohol dehydrogenase-catalyzed oxidation of mesoexo- and endo-7-oxabicyclo[2.2.1]heptane diols provides a direct one-step route to enantiomerically pure chiral γ-lactones of the oxabicyclic series.

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APA

Jones, J. B., & Francis, C. J. (1984). Enzymes in organic synthesis. 32. Stereospecific horse liver alcohol dehydrogenase-catalyzed oxidations of exo - and endo -oxabicyclic meso diols. Canadian Journal of Chemistry, 62(11), 2578–2582. https://doi.org/10.1139/v84-440

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