| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276385 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
The asymmetric synthesis of (1R,2S)-dehydrocoronamic acid ethyl ester using palladium-catalysed nucleophilic ring-opening of 3,4-epoxy-1-butene with a glycine anion equivalent as the key enantiodifferentiating step is described.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Martin E. Fox, Ian C. Lennon, Vittorio Farina,