| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278634 | Tetrahedron Letters | 2005 | 5 Pages |
Abstract
Electrooxidation of alcohols in water involving water-soluble N-oxyl compounds (WS-TEMPOs) proceeded smoothly to afford the corresponding ketones and aldehydes in good yields. Notably, most of WS-TEMPOs in water remained intact after the electrolysis. The aqueous solution containing WS-TEMPOs was recovered easily and repeatedly used for the electrooxidation of alcohols, offering a totally closed system.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jun Kubota, Yusuke Shimizu, Koichi Mitsudo, Hideo Tanaka,