| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5221415 | Tetrahedron | 2010 | 5 Pages |
Abstract
A new strategy for the stereoselective synthesis of 2-amino-2-deoxy-aldoses is described. Therefore epoxy carbamates are reacted with isocyanates to furnish urethanes, which will form the title compounds with high diastereoselectivities under basic conditions and O,O-migration of the carbamoyl group.
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Related Topics
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Organic Chemistry
