Total synthesis of methyl picrotoxate via the palladium catalyzed enyne cycloisomerization reaction
β Scribed by Michael J. Krische; Barry M. Trost
- Book ID
- 104208476
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 765 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
Abstmct: Bifurcation of the synthetic pathway affording total syntheses of picrotoxinin, picrotin and corianin from a common synthetic intermediate daived via the palladium catalyzed enyne cycloisomerization leads to the total synthesis of the picrotoxane sesquiterpene methyl picrotoxate.
π SIMILAR VOLUMES
Efficient synthesis of 7-O-methyldehydropinguisenol, a typical pinguisane-type sesquiterpene with a furan moiety, was accomplished by applying palladium-catalyzed 1,7-enyne cycloisomerization for the construction of six-membered ring bearing an exomethylene as well as of adjacent quaternary centers.
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