| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5215446 | Tetrahedron | 2014 | 9 Pages |
Abstract
A total synthesis of Daphnodorin A, a member of the Daphnodorins, was accomplished. Key features of the synthetic strategy include construction of 2-substituted-3-functionalized benzofuran via intramolecular Heck reaction and a mild Barton-McCombie deoxygenation process mediated by triethylborane. The total synthesis provided Daphnodorin A in 19.7% or 5.6% overall yield over 7 or 15 steps.
Graphical abstractDownload high-res image (137KB)Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hu Yuan, Kaijian Bi, Wanlin Chang, Rongcai Yue, Bo Li, Ji Ye, Qingyan Sun, Huizi Jin, Lei Shan, Weidong Zhang,