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The yields were significantly reduced when silyllithium 4 was generated in situ.
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Depending on the substrate, stereochemistries were proven by either X-ray crystallography, spectroscopy, or chemical correlation.
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The dimethyl acetonide protected enoate derived from D-mannitol underwent conjugate addition in a similar fashion.
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21
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0011120272
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Similar results were observed when the hydroxyl group was protected as the pivaloate ester.
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The optical activity of enoates 1c and 1e was preserved.
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