Stereoselective Synthesis of (Z)-2-Acylamido-4-phenylcrotonates

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Two practical methods for highly stereoselective synthesis of (Z)-2-acylamido-4-phenylcrotonates 2a~ b have been developed. The key step in the first route was how to control the acid-catalyzed isomerization of condensation mixtures of a -keto ester 5 with carbomite. In the second route the key step was reduction of oxime 8, derived from a -keto ester 5, with iron powder in the presence of acetic anhydride.
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