| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5284698 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
The first total synthesis of natural cytotoxic agent, sporiolide B, is described. d-Xylose was used as the chiral template to pre-control the absolute configuration during the synthesis. Yamaguchi esterification and ring closing metathesis greatly facilitate the target compound accomplishment.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Qi Chen, Yuguo Du,