Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9565187 | Tetrahedron Letters | 2005 | 5 Pages |
Abstract
Sodium benzoate reacts with α-halo-α,β-enones in the presence of tetrabutylammonium hydrogensulfate or 18-Crown-6 to afford α- and/or γ-benzoyloxylated α,β-enones in good yield. The α/γ and γ/γⲠselectivities are dependent on the substrate and reagent.
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Authors
Yujiro Hayashi, Mitsuru Shoji, Satoshi Kishida,