Catalytic Enantioselective Benzilic Ester Rearrangement
Hua Wu1, Qian Wang1, Jieping Zhu1
1Laboratory of Synthesis and Natural Products, Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne, EPFL-SB-ISIC-LSPN, BCH 5304, 1015, Lausanne, Switzerland.
Abstract:
We report the first examples of catalytic enantioselective benzilic ester rearrangement reaction. In the presence of a catalytic amount of Cu(OTf)2 and a chiral box ligand under mild conditions, reaction of 2,3-diketoesters with alcohols afforded structurally diverse α-aryl(alkyl) substituted-α-hydroxy malonates (tartronic esters) in good to excellent yields with high enantioselectivities. Preliminary mechanistic studies indicated that hemiketalization, rather than the dynamic kinetic resolution of hemiketal, was the enantiodetermining step under our reaction conditions.
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