| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279693 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
The base-catalyzed Michael addition of primary nitro compounds derived from sugars with 2 equiv of methyl vinyl ketone or acrolein was followed, in situ, by an asymmetric intramolecular aldol cyclization, thus yielding 2-acyl-4-glyco-4-nitrocyclohexanol derivatives with high diastereoselectivity.
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