| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10579527 | Tetrahedron: Asymmetry | 2011 | 5 Pages |
Abstract
The intramolecular Diels-Alder cyclization of a homochiral doubly-activated δ-pentenolide system is described, proceeding predominantly via an exo transition state to provide an advanced precursor toward unique stereochemical analogs of (+)-symbioimine.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Jason P. Burke, Michal Sabat, William H. Myers, Jason J. Chruma,