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- W2093433662 abstract "The stereoselective synthesis of the fully functionalized northern hemisphere of the marine natural product amphidinolide H2 is described. A vinylogous Mukaiyama aldol reaction and enzymatic desymmetrization of a meso compound are the key steps in the fragment synthesis. A stereoselective acetate aldol coupling and a 1,3-anti-reduction of the resulting β-hydroxy ketone complete the synthesis of the C14-C26 fragment." @default.
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- W2093433662 date "2006-08-01" @default.
- W2093433662 modified "2023-10-02" @default.
- W2093433662 title "Synthesis of the Northern Hemisphere of Amphidinolide H2" @default.
- W2093433662 doi "https://doi.org/10.1055/s-2006-942459" @default.
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