| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5291932 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
A new and readily available catalytic system has been developed to open the cyclopropane ring in [4+2+2] homo Diels-Alder cycloadducts formed by reaction of norbornadienes and 1,3-butadiene.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alexandra E. Hours, John K. Snyder,
![First Page Preview: PtCl2-Promoted cyclopropane opening in [4+2+2] homo Diels-Alder cycloadducts PtCl2-Promoted cyclopropane opening in [4+2+2] homo Diels-Alder cycloadducts](/preview/png/5291932.png)