| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5283011 | Tetrahedron Letters | 2006 | 6 Pages |
Abstract
The C1-C11 fragment of caribenolide I was prepared from 3-paramethoxybenzyloxypropanal, with an excellent control of the configuration of stereogenic centres. The key steps rely on an asymmetric aldolisation and a Baylis-Hillman reaction.
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Authors
Matar Seck, Xavier Franck, Blandine Seon-Meniel, Reynald Hocquemiller, Bruno Figadère,