An efficient and stereoselective construction of the core structure of the manzamines via an intramolecular Michael reaction
β Scribed by K.M.J. Brands; L.M. DiMichele
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 230 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A strategically functionalized tricyclic subunit of the manzamines was efficiently synthesized with complete stereochemical control using a combination of an intramolecular Michael reaction of a pyroglutamic acid derivative and a hydrogenation.
π SIMILAR VOLUMES
The highly functionalized aryl core structure of balanol has been synthosized employing a mgioselective intramolecular Heck reaction as the key step. This approach can potentially lead to new types of analogues of the potent PKC inhibitor.
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