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- W2949761256 abstract "The response of the rate of triethylamine-induced dehydroacetoxylation of methyl threo-3-acetoxy-2-halogeno-3-phenylpropanoate to the influence of substituents in the leaving group points to a change in mechanism from (E1 cB)I to a concerted process of the carbanion type. On the other hand, the erythro-isomers seem to undergo elimination exclusively through a carbanionic pathway. The effect of the acetoxy substituents upon the competitive transesterification is discussed." @default.
- W2949761256 created "2019-06-27" @default.
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- W2949761256 date "1988-12-27" @default.
- W2949761256 modified "2023-09-25" @default.
- W2949761256 title "ChemInform Abstract: Dehydroacetoxylation and Acetate Transesterification in the Reactions of erythro- and threo-Methyl 3-(Substituted acetoxy)-2-halogeno-3-phenylpropanoates with Triethylamine." @default.
- W2949761256 cites W2035833621 @default.
- W2949761256 doi "https://doi.org/10.1002/chin.198852076" @default.
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