Synfacts 2006(5): 0419-0419  
DOI: 10.1055/s-2006-934395
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart · New York

Synthesis of (-)-α-Kainic Acid

Contributor(s): Philip Kocienski
J.-F. Poisson*, A. Orellana, A. E. Greene
Université Joseph Fourier, Grenoble, France
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Publikationsverlauf

Publikationsdatum:
21. April 2006 (online)

Significance

Kainic acid is used to reproduce neuronal cell death for the study of Alzheimer’s disease and epilepsy. Its supply from the natural source (the alga Digenea simplex) is intermittent and hence there is a spur for a good synthesis. There are now 19 total syntheses and five formal syntheses of (-)-Kainic acid but efficiency and scalability remain elusive. The present synthesis for the first time uses trans-4-hydroxy-l-proline (A) as the starting material. A noteworthy step is the nucleophilic substitution of a secondary tosylate by an alkenylcuprate (G to H) with retention of configuration.