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- W2024294992 endingPage "1706" @default.
- W2024294992 startingPage "1703" @default.
- W2024294992 abstract "Methyl 4-hydroxy-E-2-alkenoates prepared from aldehydes in one step, undergo the Michael reactions with thiolate anions to give 4-alkanolide derivatives, which are converted into 2-alken-4-olides. Methyl 4-methanesulfonyloxy-E-2-alkenoates undergo the substitution reactions, and subsequent treatments give methyl E,E-2,4-alkadienoates." @default.
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- W2024294992 date "1982-11-05" @default.
- W2024294992 modified "2023-09-27" @default.
- W2024294992 title "SELECTIVE REACTIONS OF THIOLATE ANIONS WITH 4-HYDROXY-<i>E</i>-2-ALKENOIC ESTERS OR 4-METHANESULFONYLOXY-<i>E</i>-2-ALKENOIC ESTERS. SYNTHESIS OF 2-ALKEN-4-OLIDES (Δ<sup>α,β</sup>-BUTENOLIDES) AND<i>E</i>,<i>E</i>-2,4-ALKADIENOIC ESTERS" @default.
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- W2024294992 doi "https://doi.org/10.1246/cl.1982.1703" @default.
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