Silver carbonate is the most common silver additive in palladium-catalysed C–H activation and functionalisation. It is a weak, insoluble base that is compatible with sensitive functional groups, it abstracts halide from palladium(II) intermediates to open a coordination site, and in Fujiwara–Moritani olefinations and related Pd(II)/Pd(0) cycles it acts as the terminal oxidant that returns palladium(0) to palladium(II). Typical loadings are 1–2 equivalents relative to the substrate.
In carbohydrate chemistry it is the classical promoter of the Koenigs–Knorr glycosylation: the glycosyl bromide is activated by silver carbonate, with or without silver perchlorate or molecular sieves, to give the glycoside with high stereoselectivity. Precipitated onto Celite it becomes Fétizon's reagent, which oxidises primary and secondary alcohols selectively to aldehydes and ketones in refluxing benzene or toluene without over-oxidation and without touching most other functional groups.
Silver carbonate is also used to prepare silver carboxylates and other silver(I) salts by reaction with the corresponding acid (with evolution of carbon dioxide), as a halide scavenger to generate cationic rhodium, iridium and gold catalysts, and as a mild silver source in the synthesis of silver nanoparticles and supported silver catalysts.