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Total Synthesis of (−)-Kainic Acid via Intramolecular Michael Addition: A Second-Generation Route

✍ Scribed by Sakaguchi, Hiroshi; Tokuyama, Hidetoshi; Fukuyama, Tohru

Book ID
121717432
Publisher
American Chemical Society
Year
2008
Tongue
English
Weight
113 KB
Volume
10
Category
Article
ISSN
1523-7060

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Stereocontrolled Total Synthesis of (±)-Culmorin via the Intramolecular Double Michael Addition. -The stereocontrolled total synthesis of racemic culmorin (VII) is based on the intramolecular double Michael addition of the cyclopentenone (V) having an α,β-unsaturated ester moiety. -