Abstract
A group of soluble polymer-supported chiral tartrate ligands was prepared by liquid-phase synthesis with ligand diversity strategy. Moderate to excellent chemical yields and enantiomeric excesses were obtained by using soluble polymer-supported tartrate ester in asymmetric oxidation of prochiral sulfides using Ti(O-i-Pr)4/cumyl hydroperoxide, and the workup was greatly simplified. The influence of substituent in chiral tartrate ligands on the enantioselectivities of the reaction was disclosed.
Original language | English |
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Pages (from-to) | 8453-8455 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 48 |
Issue number | 48 |
DOIs | |
State | Published - 26 Nov 2007 |