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The title compound, C15H24O5, was isolated from the flowers of Parthenium hysterophorus. The crystal structure determination confirms the relative stereochemistry unambiguously. The packing is stabilized by O—H...O hydrogen bonding.

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The structure of the clerodane diterpene C21H30O5, with modest antibacterial activity and isolated from the plant Pulicaria wightiana, was established to be meth­yl 6α-hydr­oxy-3,13-clerodadien-15,16-olid-18-oate. The fused six-membered rings of the deca­lin system have sofa and chair conformations. The furan­one side chain is in an antiperiplanar conformation. The mol­ecules in the crystal structure are stabilized by an intra­molecular O—H...O hydrogen bond and a chain of inter­molecular C—H...O inter­actions.
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