| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223836 | Tetrahedron | 2010 | 6 Pages |
Abstract
A synthesis of the β-lactone esterase inhibitors (−)-ebelactones A and B is described. The synthesis features the use of a Hoppe homoaldol reaction and a Cu(I)-mediated 1,2-metallate rearrangement of a metallated enol carbamate as key fragment linkage reactions.
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