| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5287683 | Tetrahedron Letters | 2005 | 5 Pages |
Abstract
Bicyclo[2.2.2]oct-5-en-2-ones 19 can be made in a one-pot process from ketones 18 and cyclohexenone 6 in strong acid.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Synthesis of bicyclo[2.2.2]oct-5-en-2-ones via a tandem intermolecular Michael addition intramolecular aldol process (a bridged Robinson annulation)](/preview/png/5287683.png "First Page Preview: Synthesis of bicyclo[2.2.2]oct-5-en-2-ones via a tandem intermolecular Michael addition intramolecular aldol process (a bridged Robinson annulation)")
Authors
Michael E. Jung, Andreas Maderna,