| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5285368 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
A highly selective synthesis of the enol triflate derived from the 9-keto group was achieved directly from diketones in kinetic conditions. The isomeric triflates were also prepared selectively in other conditions (kinetic or thermodynamic) and their specific Stille couplings achieved.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Nicolas Zorn, Robert Lett,