| Literature DB >> 21288725 |
Ricardo F Schumacher1, Alisson R Rosário, Ana C G Souza, Carmine I Acker, Cristina W Nogueira, Gilson Zeni.
Abstract
Here we present our results in palladium cross-coupling reaction of aryl boronic acids with 4-iodo-2,3-dihydroselenophene derivatives. The cross-coupled products were obtained in satisfactory yields. A dehydrogenation of 4,5-diphenyl-2,3-dihydroselenophene was activated by DDQ and the 2,3-diarylselenophene was obtained in good yield. Regarding the antioxidant activity, the selenophene derivative 3a was effective in counteracting lipid and protein oxidation as well as scavenging ABTS radical. The findings of the present study indicate that 3a is a prototype for future drug development programs to treat disorders mediated by reactive oxygen species.Entities:
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Year: 2011 PMID: 21288725 DOI: 10.1016/j.bmc.2011.01.005
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641