Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1385343 | Carbohydrate Research | 2008 | 13 Pages |
Abstract
The first example of a non-enzymatic C-2 epimerization of aldonolactones is reported. The reaction of 2,3,4,6-tetra-O-benzyl-d-gluconolactone or 2,3,4,6-tetra-O-benzyl-d-mannonolactone with MgI2 in EtOH afforded their respective C-2 epimer. Studies conducted in EtOD showing the incorporation of a deuterium atom only at the C-2 position of the epimerized product reveal an epimerization rather than a racemization reaction. A mechanism involving a chelation with a magnesium species is proposed to explain this C-2 inversion reaction.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Julie Gratien, Marie-Pierre Heck, Charles Mioskowski,