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Total Synthesis of (−)-Samaderine Y from (S)-(+)-Carvone

✍ Scribed by Tony K. M. Shing; Ying Y. Yeung

Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
116 KB
Volume
44
Category
Article
ISSN
0044-8249

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✦ Synopsis

Quassinoids, a group of heavily oxygenated terpenoid bitter compounds isolated from the Simaroubaceae plant family, display a wide range of biological activities [1] and have attracted interest with respect to their synthesis during the past decades. [2] (À)-Samaderine Y (1), a pentacyclic quassinoid isolated from Quassia indica, was shown to exhibit in

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Total Synthesis of (−)-Samaderine Y from
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✍ Tony K. M. Shing; Ying Y. Yeung 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 115 KB 👁 1 views

Quassinoids, a group of heavily oxygenated terpenoid bitter compounds isolated from the Simaroubaceae plant family, display a wide range of biological activities [1] and have attracted interest with respect to their synthesis during the past decades. [2] (À)-Samaderine Y (1), a pentacyclic quassinoi

ChemInform Abstract: Enantiocontrolled F
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Enantiocontrolled Formal Total Synthesis of Paeonilactone A and B from (S)-(+)-Carvone. -Compound (V), which is an intermediate in the synthesis of paeonilactone A and B, is prepared via stereoselective palladiumcatalyzed oxylactonization of diene (IV) as the key step. -(ROENN, M.;