| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9565195 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
The singlet oxygen photooxidations of several carboxylic acid salts were conducted in deuterated water. We attribute the observed regiochemistry to stabilizing hydrogen bonding interactions between the solvent and the perepoxide, which leads to the major ene product.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kristina L. Stensaas, Anisha Bajaj, Akram Al-Turk,