A Synthesis of Protoanemonin. The Tautomerism of Acetylacrylic Acid and of Penicillic Acid

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Abstract

Protoanemonin is formed by the action of acetic anhydride on acetylacrylic acid in the presence of an acid catalyst. Spectroscopic data on the ring-chain tautomerism of acetylacrylic acid and of penicillic acid are given. © 1946, American Chemical Society. All rights reserved.

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Shaw, E. (1946). A Synthesis of Protoanemonin. The Tautomerism of Acetylacrylic Acid and of Penicillic Acid. Journal of the American Chemical Society, 68(12), 2510–2513. https://doi.org/10.1021/ja01216a024

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