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- W2072830863 abstract "Elimination reactions of enol sulphonates have been further studied. The enol sulphonates of p-anisolyl-, 2-furoyl-, and 2-thenoyl-malonic esters readily gave the corresponding propiolic acids on treatment with base, whereas the enol sulphonates of o-, m-, and p-nitrobenzoylmalonic esters gave negligible yields. The enol sulphonates of cyclopropylcarbonylmalonate gave cyclopropylpropiolic acid, while those of trichloroacetylmalonate and fumaroylmalonate gave no acetylenic product. The enol sulphonates of tribenzoylmethane gave benzoylphenyl-acetylene." @default.
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- W2072830863 date "1966-01-01" @default.
- W2072830863 modified "2023-09-23" @default.
- W2072830863 title "Enol elimination reactions. Part III. The scope and limitations of eliminations involving enol sulphonates" @default.
- W2072830863 doi "https://doi.org/10.1039/j39660001390" @default.
- W2072830863 hasPublicationYear "1966" @default.
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