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As in the case of microcarpalide, catalyst Ru-II provided only the undesired Z-23 in 72% yield. Again, the preferential formation of the more stable Z-isomer is due to thermodynamic control of the RCM process by catalyst Ru-II.
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After selective cleavage of the MOM group in olefin Z-23, crystalline hydroxy lactone Z-24 was formed in 70% yield. Its structure and absolute configuration were confirmed by means of an X-ray diffraction analysis. (Chemical Equation Presented)
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Compound 46 was obtained a ca. 2:1 mixture of anomers, each of them being a ca. 9:1 mixture of E/Z isomers.
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