Asymmetric synthesis of the core structure of the Melodinus alkaloids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Methyleneindolines, indolenines, and indoleniniums. 18. A biomimetic entry in the Melodinus alkaloids
2. Methyleneindolines, indolenines, and indoleniniums. 20. The first biomimetic synthesis of scandine and meloscine
3. The first skeletal rearrangement of Aspidosperma to Melodinus alkaloids. A facile conversion of (-)-vincadifformine into N-methyltetrahydromeloscine
4. Use of aza-Cope rearrangement-Mannich cyclization reactions to achieve a general entry to Melodinus and Aspidosperma alkaloids. Stereocontrolled total syntheses of (.+-.)-deoxoapodine, (.+-.)-meloscine, and (.+-.)-epimeloscine and a formal synthesis of (.+-.)-1-acetylaspidoalbidine
5. First Asymmetric Synthesis of a Hasubanan Alkaloid. Total Synthesis of (+)-Cepharamine
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