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Stereocontrolled Total Synthesis of (±)-Culmorin via the Intramolecular Double Michael Addition

✍ Scribed by Takasu, Kiyosei; Mizutani, Sayaka; Noguchi, Miho; Makita, Kei; Ihara, Masataka

Book ID
126820026
Publisher
American Chemical Society
Year
1999
Tongue
English
Weight
53 KB
Volume
1
Category
Article
ISSN
1523-7060

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ChemInform Abstract: Stereocontrolled To
ChemInform Abstract: Stereocontrolled Total Synthesis of (.+-.)-Culmorin via the Intramolecular Double Michael Addition.
✍ Kiyosei Takasu; Sayaka Mizutani; Miho Noguchi; Kei Makita; Masataka Ihara 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

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. -