A simple, fast and reliable method was developed for the analysis ofjinggangmycin A (validamycin A) in commercial formulations. The running buffer used was acet
Novel C-nucleosides of tiazofurin analogue (2-[2-(hydroxymethyl)-1,3-dioxolan-5-yl] 1,3-thiazole-4-carboxamide) and its thiol-substituted derivative (2-[2-(merc
1,1-Diphenyl-2, 2-dicyanoethylene reacts with 10-methyl-9, 10-dihydroacridine in deaerated acetonitrile under irradiation with λ>320nm to give the coupling pro