Published April 30, 2020
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Fig. 4. A in Molecular cloning and functional characterization of a two highly stereoselective borneol dehydrogenases from Salvia officinalis L
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- 1. ∗ & Institute of Molecular Biotechnology, Graz University of Technology, Petersgasse 14, 8010, Graz, Austria
Description
Fig. 4. A) Selective oxidative kinetic resolution of borneol enantiomers (+)-1 and (−)-1 and B) isoborneol enantiomers (+)-2 and (−)-2 to corresponding camphor enantiomers 3. The selective oxidation of (+)-borneol ((+)-1) leads to (+)-camphor ((+)-3), while selective oxidation of (+)-isoborneol leads to (−)-camphor (−)-3).
Notes
Published as part of Drienovská, Ivana, Kolanović, Dajana, Chánique, Andrea, Sieber, Volker, Hofer, Michael & Kourist, Robert, 2020, Molecular cloning and functional characterization of a two highly stereoselective borneol dehydrogenases from Salvia officinalis L, pp. 1-8 in Phytochemistry (112227) 172 on page 4, DOI: 10.1016/j.phytochem.2019.112227, http://zenodo.org/record/8294329
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- Journal article: 10.1016/j.phytochem.2019.112227 (DOI)
- Journal article: urn:lsid:plazi.org:pub:FFEEFFD6FFB7746EFFD6BE1FFD2E5353 (LSID)
- Journal article: https://zenodo.org/record/8294329 (URL)