Enantio- and stereoselective syntheses of monodeuterium-labeled glycerols

Article abstract of DOI:10.1271/bbb.61.1038

An efficient method is described for synthesizing and four possible diastereomers of stereochemically defined monodeuterated glycerols by utilizing Sharpless asymmetric dihydroxylation.

Full text of DOI:10.1271/bbb.61.1038

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Bioscience, Biotechnology, and Biochemistry
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Enantio- and Stereoselective Syntheses of
Monodeuterium-labeled Glycerols
Kenji Yagia, Hideaki Oikawaa & Akitami Ichiharaa
a Department of Bioscience and Chemistry, Faculty of Agriculture, Hokkaido University,
Sapporo 060, Japan
Published online: 12 Jun 2014.
To cite this article: Kenji Yagi, Hideaki Oikawa & Akitami Ichihara (1997) Enantio- and Stereoselective Syntheses
of Monodeuterium-labeled Glycerols, Bioscience, Biotechnology, and Biochemistry, 61:6, 1038-1040, DOI: 10.1271/
bbb.61.1038
To link to this article: http://dx.doi.org/10.1271/bbb.61.1038
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