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Synthetic studies on brevetoxin-B. Part 1: Stereoselective synthesis of the ABC-ring system
β Scribed by Goh Matsuo; Hiroko Matsukura; Nobuyuki Hori; Tadashi Nakata
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 107 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
The IJK-ring system of brevetoxin-B was stereoselectively synthesized based on the 6-endo-cyclizations of a hydroxy methylepoxide and a hydroxy styrylepoxide, and the direct introduction of the C-4 unit as the side chain.
A new method for constructing the ABCE ring system of azadirachtin in a stereoselective manner was developed. The synthesis of the model compound features (1) stereoselective construction of the highly hindered C8 quaternary center by an intermolecular addition reaction of an allylborane with an ald