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https://doi.org/10.1002/chin.201504026
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Cite Journal: ChemInform |  Publication Date: Jan 1, 2015 |
Affiliation: Tokyo University of Pharmacy and Life Sciences
AbstractThe corresponding Michael‐adducts are formed with high yields and enantioselectivities (up to 99% e.e.).The excellent performance of the catalyst is probably due to the ability of the perfluoroalkyl group to function as a preferable hydrophobic reaction field in water and its strong electron‐withdrawing nature.
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