Abstract

The efficient trifluoromethylation of a series of carbonyl-containing lignin model compounds was made possible by using Ruppert' s reagent in the presence of tetramethylammonium fluoride (TMAF), followed by hydrolysis with aqueous HF. These studies demonstrate that such a method can quantitatively convert carbonyl groups to the CF 3-containing compounds, thus qualifying the procedure as a potential analytical tool for the determination of carbonyl groups in lignins.

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