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A series of (5-nitrofuran-2-yl)-1, 3, 4-thiadiazole-2-yl derivatives 6a–6e have been synthesized and screened for in vitro anti-leishmanial activity against the promastigote form of L. major. The structure of Schiff bases were confirmed by 1H NMR, IR. Screening results indicate that all of the designed and synthesized final compounds (6a-6e) significantly reduced the viability of promastigotes ...
Urazolyl radicals are a class of persistent nitrogen-centered radicals. In previous work, we successfully formed self-assembled monolayers substituted urazolyl on gold surfaces. To extend the scope these investigations, sought to form monolayer using radical species that knew existed predominantly in dimerized N-N instead existing as free N-centered species, had previously been investigated. We...
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