Asymmetric reduction of perfluoroalkyl ketones with chiral lithium alkoxides |
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Authors: | Yasser Samir Sokeirik Itsumaro Kumadaki |
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Affiliation: | Faculty of Pharmaceutical Sciences, Setsunan University, 45-1, Nagaotoge-cho, Hirakata 573-0101, Japan |
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Abstract: | Reduction of perfluoroalkyl ketones with chiral lithium alkoxides gave chiral α-perfluoroalkyl alcohols in high enantiomeric excesses. Interestingly, reaction of 2,2,2-trifluoroacetophenone (1) with lithium (S)-1-phenylethoxide (2) gave (S)-2,2,2-trifluoro-1-phenylethanol (3), while the same reaction of perfluorooctan-1-one (7) with 2 gave (R)-1H-1-phenylperfluorooctanol (8). Based on the speculation of mechanism, the order of steric effects on this reaction is estimated as C7F15 > substituted phenyl > CF3. |
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Keywords: | Asymmetric reduction Chiral transfer Perfluoroalkyl ketone Lithium alkoxide α-(Perfluoroalkyl)carbinol 1-Phenylethanol Trifluoroacetophenone Steric effect |
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