| Literature DB >> 1403685 |
F Boscá1, R Martínez-Máñez, M A Miranda, J Primo, J Soto, L Vañó.
Abstract
The decarboxylation of naproxen (1H) and its salt (1-) was achieved by means of chemical [Ce(IV) or S2O8(2-)] and electrochemical oxidation. The product patterns were compatible with mechanisms involving single-electron transfer from the pi-system or the carboxylate moiety. The results are discussed in connection with the involvement of electron-transfer processes in the reported phototoxicity of naproxen.Entities:
Mesh：
Substances：
Year: 1992 PMID： 1403685 DOI： 10.1002/jps.2600810519
Source DB: PubMed Journal: J Pharm Sci ISSN： 0022-3549 Impact factor: 3.534