A general synthetic route towards bastadins. Part 1: Synthesis of the eastern part of bastadins 4–16
✍ Scribed by Elias A. Couladouros; Vassilios I. Moutsos
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 276 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A general synthetic route for the construction of the eastern part of the macrocyclic bastadins 4-16 is presented. The brominated biaryl ethers are synthesized using the iodonium salt method. The synthesis is accomplished within 18 steps in 15.5% overall yield.
📜 SIMILAR VOLUMES
A general synthetic route for the construction of the western part of the macrocyclic bastadins 4-16 is presented. The western and the eastern segments were coupled using the imidazolide of the corresponding acid. The bromine at position y2 may be added at this advanced step regiospecifically, stren
Towards a Versatile Synthesis of Kainoids. Part 1. Introduction of the C-3 and C-4 Substituents. -Starting from trans-4-hydroxy-Lproline, an enamine alkylation is used for the stereospecific introduction of the C-3 substituent of acromelic acid analogues. For the introduction of C-4 aryl substituen
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