Total synthesis of (+)-epiquinamide from d-mannitol
โ Scribed by Subhash Ghosh; J. Shashidhar
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 154 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The total synthesis of (+)-epiquinamide, a novel quinolizidine alkaloid isolated from the Ecuadoran poison frog, Epipedobates tricolor is described. The key step includes a ring-closing metathesis reaction to construct both the six member rings. D-Mannitol was used as a chiral pool material.
๐ SIMILAR VOLUMES
A total convergent synthesis of leukotriene (+)-LTB4 has been carried out via two enantiomerically pure CY-hydroxyaldehydes,chiral key intermediates both obtained from D-mannitol and connected at a four carbon atoms interval by Wittig reactions. f)J. Rokach, J. Adams. Act. Res.,
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