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- W4252321268 abstract "Ohne das Ketalisomer: Der 2,8-Dioxabicyclo[3.2.1]octan-Kern der Saragossasäure C (1) wurde durch die Rh-katalysierte 1,3-dipolare Cycloaddition eines Alkins an ein Estercarbonylylid aufgebaut. Ein weiterer Vorzug dieser verbesserten Synthese ist die Einführung der Alkylseitenkette an C1 durch Olefinkreuzmetathese." @default.
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- W4252321268 date "2003-11-04" @default.
- W4252321268 modified "2023-10-17" @default.
- W4252321268 title "Total Synthesis of the Squalene Synthase Inhibitor Zaragozic Acid C by a Carbonyl Ylide Cycloaddition Strategy" @default.
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- W4252321268 doi "https://doi.org/10.1002/ange.200352629" @default.
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