The ester enolate claisen rearrangement of allyl α-hydroxyacetates and α-phenylthioacetates |
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| Authors: | David J. Ager Richard C. Cookson |
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| Affiliation: | Department of Organic Chemistry, Robert Robinson Laboratories, P.O. Box 147, Liverpool, L69 3BX U.K.;Department of Chemistry, The University, Southampton SO9 5NH U.K. |
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| Abstract: | The ester enolates of allylα-hydroxyacetates and α-phenylthioacetates undergo a Claisen rearrangement to give α-substituted-γ,δ-unsaturated acids. |
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