Boron trifluoride mercury trifluoroacetate

The mixture of mercury oxide, boron trifluoride-ether, and trifluoroacetic acid is a particularly effective catalyst for hydration of alkynes 84 mixtures of mercury oxide and boron trifluoride88 and of mercury oxide with sulfuric acid86 have also been used. Addition to acid-sensitive acetylenes is carried out under neutral conditions by means of mercuriacetamide or mercuri-/7-toluenesulfonamide.87 Acid exchange resins loaded with mercury ions can also be used for addition of water to alkynes.88... 

Lithium tetrafluoroborate in wet acetonitrile has been described as an effective combination for the hydrolysis of acetals under mild weakly acidic conditions. Dithians were unaffected. Methods for the hydrolysis of thioacetals continue to appear. Reagents that have been described include a polystyryl-mercury(n) trifluoroacetate combination, which retains the metal on the resin, lead(iv) dioxide and boron trifluoride etherate, aqueous hydrochloric acid in dioxan containing dimethyl sulphoxide, methyl-bis(methylthio)sulphonium hexa-chloroantimonate, and iodoxybenzene, catalysed by toluene-p-sulphonic acid. Dithioacetals derived from ethane-1,2-dithiol may be cleaved with dimethyl sulphoxide in combination with either t-butyl or trimethylsilyl bromides and iodides. Regeneration of ketones from ethanediyl-S S -acetals via the lithium-di-isopropylamide-promoted fragmentation to the thioketone and subsequent hydrolytic work-up only gives satisfactory yields for aryl methylketone derivatives. Dithioacetal SS-dioxides are rapidly cleaved in hot methanolic hydrochloric acid solution. ... 

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