Syntheses of (卤)-Serratine, (卤)-Lycoposerramine T, and (卤)-Lycopoclavamine B
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The first total syntheses of (卤)-serratine, (卤)-lycoposerramine T, and (卤)-lycopoclavamine B have been accomplished. The functionalized octahydroindane skeleton of these natural products was constructed by an efficient Diels鈥揂lder reaction of an 伪-alkynylcyclopentenone and the stereoselective introduction of a tertiary hydroxyl group. Two of these natural products were divergently synthesized from the same synthetic intermediate at a later stage.

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