Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5220162 | Tetrahedron | 2012 | 9 Pages |
Abstract
An efficient route to orthogonally protected l-glucose, l-mannose, and l-galactose is described. Using the strategy to switch the functional groups at C1 and C5 of d-glucose, l-glucose is obtained via a key intermediate C-glycoside. Preparations of l-mannose and l-galactose derivatives from the orthogonally protected l-glucose were accomplished in good yields using the Lattrell–Dax method.
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