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The fluoride ion effect in the reactions of singlet oxygen with enols
Authors:Harry H. Wasserman  James E. Pickett
Affiliation:Department of Chemistry, Yale University, New Haven CT 06511, U.S.A.
Abstract:The fluoride ion effect in the reactions of enolic systems with singlet oxygen has been investigated. β-Dicarbonyl compounds yielded 1,2,3-tricarbonyl derivatives, some of which underwent further hydration, whereas α-diketones suffered oxidative decarboxylation to give open-chain aldehydo-acids or keto-acids.
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