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2O (5 mol%). The resulting mixture was allotted to react under stirring at r.t. or at 30°C and the reaction was monitored by TLC or GC-MS. After completion, the solvent was removed by evaporation. To the residue, acetone (few mL) was added to precipitate the catalyst, which was separated by filtration. The filtrate was concentrated and the crude products were purified by chromatography on silica gel (230-400 mesh) eluting with n-hexane/EtOAc mixtures.
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