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- W2950989843 abstract "Enantioselective protonation of a simple enolate has been developed using an optically pure γ-hydroxyselenoxide 1 as a chiral proton source. Reaction of zinc bromide enolate 7b with (SSe)-selenoxide (SSe)-1c gave (S)-2-benzylcyclohexanone (S)-8 with high enantioselectivity. Intramolecular hydrogen bonding between hydroxy group and seleninyl-oxygen of 1 would contribute to this asymmetric induction." @default.
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- W2950989843 date "1996-03-01" @default.
- W2950989843 modified "2023-10-12" @default.
- W2950989843 title "The First Example of Enantioselective Protonation of Prochiral Enolates with Chiral<i>γ</i>-Hydroxyselenoxides" @default.
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- W2950989843 doi "https://doi.org/10.1246/cl.1996.207" @default.
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