| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277991 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Photochemical acylations of 2-substituted-1,4-naphthoquinones with various aldehydes furnished acylated hydroquinones and acylated quinones in moderate to good combined yields. All reactions are easily performed and open a rapid access to biologically active compounds. For the 2-methyl-1,4-naphthoquinone/butyraldehyde pair, a novel tri-keto compound has been additionally isolated.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Prashant A. Waske, Jochen Mattay, Michael Oelgemöller,