Highly Enantioselective Catalytic Allylboration of Ketiminoesters: Practical and Scalable Synthesis of α-Fully-Substituted Amino Esters
2019-07-24T12:11:20Z (GMT) by
We report the first catalytic enantioselective allylboration of α-ketiminoesters to afford chiral α-allyl-α-aryl and α-allyl-α-trifluoromethyl amino esters in excellent isolated yields and with high optical purity. This operationally simple allylation proceeds under ambient conditions with indium(I)-iodide/BOX-type ligand (5–10 mol%) and can be performed on a gram scale. A proposed qualitative model for the high stereoselectivity indicates that the origin of selectivity is likely due to attractive interactions between the substrate and the BOX ligand. Using a different BOX-type ligand reverses the reaction’s absolute sense of enantioselectivity. The allylated products are easily converted to enantiomerically enriched α-substituted proline derivatives.