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- W2912771631 abstract "The electrochemical behavior of osmociphenol (3, Oc-OH), an organometallic osmium-based anticancer drug candidate, has been investigated by cyclic voltammetry in the absence and presence of lutidine used as a base model. Osmociphenol exhibited spontaneous deprotonation of the phenol function upon oxidation of the osmocene moiety due to its high acidity. In the presence of lutidine, a base-dependent and different electrochemical behavior was observed at low scan rates indicating a second oxidation step leading to the corresponding cationic quinone methide precursor (3b+). However, compared to ruthenocene derivatives, the stability of 3b+ prevented its conversion into quinone methide as the final and stable complex. Despite differences in their oxidative processes, osmociphenol and ruthenociphenol derivatives exhibit similar biological activities." @default.
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- W2912771631 date "2019-04-01" @default.
- W2912771631 modified "2023-10-17" @default.
- W2912771631 title "New mechanistic insights into osmium-based tamoxifen derivatives" @default.
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- W2912771631 doi "https://doi.org/10.1016/j.electacta.2019.02.019" @default.
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