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Issue 1, 1969
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Rearrangement of aryl halogenoacetates during nucleophilic substitution

Abstract

The reaction between aryl halogenoacetates and alcohols or phenols in acetone containing potassium carbonate leads to derivatives in which the more basic nucleophile is attached to the carbonyl group. Rearrangement occurs if necessary to produce this derivative.

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Article information


J. Chem. Soc. C, 1969, 37-39
Article type
Paper

Rearrangement of aryl halogenoacetates during nucleophilic substitution

F. S. H. Head and G. Lund, J. Chem. Soc. C, 1969, 37
DOI: 10.1039/J39690000037

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