| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5229696 | Tetrahedron | 2006 | 5 Pages |
Abstract
A diastereoselective total synthesis of (±)-canadensolide is described. The key step is to introduce the α-methylene group by the ozonolysis of mono-substituted alkenes followed by reaction with a preheated mixture of CH2Br2-Et2NH.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yung-Son Hon, Cheng-Han Hsieh,