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- W2023646835 abstract "Reactivity comparison, Arrhenius parameters, and trapping of the above-depicted unsaturated intermediate strongly suggest that the alkaline hydrolysis of the title ester follows a mechanism of the E1cB type. This is the first observation of the occurrence of a dissociative route in the hydrolysis of an acyl derivative with three π-systems interposed between the hydroxyl group (the internal nucleophile upon ionization) and the reaction center. Comparison with the hydrolysis of 2,4-dinitrophenyl 4‘-hydroxybenzoate shows that interposition of the vinylenic groups is beneficial to the dissociative route." @default.
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- W2023646835 date "1999-09-23" @default.
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- W2023646835 title "A New, “Elongated” Oxo Ketene Intermediate in the Dissociative Hydrolysis of 2,4-Dinitrophenyl (2E,4E)-5-(4‘-Hydroxyphenyl)pentadienoate" @default.
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- W2023646835 doi "https://doi.org/10.1021/ol990796a" @default.
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