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- W1981379259 abstract "Eleven β-hydroxy selenides were kinetically resolved using an immobilized lipase (Amano PS-C II) in toluene in the presence of vinyl acetate at 30 °C. This approach provided, in several cases, both enantiomers in high enantiomeric excess. The role of the size of substituents and the behaviour of cyclic β-hydroxy selenides is also discussed. Enantiopure β-hydroxy selenides are useful building blocks. As an application of this chemistry, enantiopure (1S,2R)-indene oxide was obtained in one step from the proper enantiopure β-hydroxy selenide." @default.
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- W1981379259 date "2006-10-01" @default.
- W1981379259 modified "2023-09-27" @default.
- W1981379259 title "Lipase-catalyzed resolution of β-hydroxy selenides" @default.
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- W1981379259 doi "https://doi.org/10.1016/j.tetasy.2006.10.010" @default.
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