A Highly Diastereoselective Decarboxylative Mannich Reaction of β-Keto Acids with Optically Active <i>N</i>-Sulfinyl α-Imino Esters
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A range of protected γ-oxo-α-amino esters have been prepared in a highly regio- and stereoselective manner through the decarboxylative Mannich reaction of β-keto acids with optically active N-tert-butanesulfinyl α-imino esters in the presence of 3 mol % La(OTf)3 or 5 mol % Y(OTf)3 at 20 °C. Preliminary mechanistic studies indicate that the reaction proceeds through imine addition followed by decarboxylation.
创建时间:
2012-06-15



