| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5285672 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
The first total synthesis of bhimamycin B was achieved by oxidative skeletal rearrangement of 4-acetylnaphtho[1,2-b]furan-5-ol with PhI(OAc)2.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Synthesis of bhimamycin B based on oxidative rearrangement of 4-acetylnaphtho[1,2-b]furan-5-ol to naphtho[2,3-c]furan-4,9-dione](/preview/png/5285672.png "First Page Preview: Synthesis of bhimamycin B based on oxidative rearrangement of 4-acetylnaphtho[1,2-b]furan-5-ol to naphtho[2,3-c]furan-4,9-dione")
Authors
Hidemitsu Uno, Seiya Murakami, Akiko Fujimoto, Youtarou Yamaoka,