| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5280840 | Tetrahedron Letters | 2010 | 5 Pages |
Abstract
A new divergent total synthesis of the cuparenic sesquiterpenes enokipodins A and B is described. It features as the key step a novel cation-controlled, palladium (II) improved, 5-endo cyclization, which has been classically considered as 'non-favoured'.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jesús Armando Luján-Montelongo, José G. Ávila-Zárraga,