| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5227995 | Tetrahedron | 2008 | 6 Pages |
Abstract
Application of a sequential nickel-catalyzed reductive aldol cyclization–lactonization reaction in a short formal synthesis of salinsporamide A, a potent 20S proteasome inhibitor and anti-cancer compound, is described.
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