| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5224081 | Tetrahedron | 2008 | 6 Pages |
Abstract
A combination of Ireland ester Claisen rearrangement and intramolecular type II carbonyl ene reactions were exploited for the total synthesis of chamigrenes containing a quaternary carbon atom next to the spirocentre in spiro[5.5]undecane.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
A. Srikrishna, R. Ramesh Babu,