posted on 2009-12-08, 16:23authored byJohn Fawcett, Eric G. Hope, Alison M. Stuart, Andrew J. West
After the asymmetric addition of allyltri-n-butyltin to benzaldehyde, a perfluoroalkylated BINOL-Sn complex was separated from the organic product using fluorous reverse phase silica gel. The lightly fluorinated ligand was then recovered by hydrolysis of the R[subscript f6]-BINOL-Sn complex with dilute hydrochloric acid and was reused three times without loss of activity or enantioselectivity.