Skip to main content
Journal ArticleOPEN ACCESS

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
N/ACitations
Citations of this article
5Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free