| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5283574 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
A convergent synthesis of the FGHI ring segment of yessotoxin was achieved via the intramolecular allylation of an α-chloroacetoxy ether and subsequent ring-closing metathesis.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Isao Kadota, Hirokazu Ueno, Yuki Sato, Yoshinori Yamamoto,