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<p> Many focused on the hydroxypalladation step, which forms the C&ndash;O bond.  Early reactions used conditions much milder than the industrial plants and obtained contradictory results; the modern consensus is that the step's stereochemistry is quite sensitive to chloride concentrations.</p>

<p>Other studies investigated reaction's application to more complex <a href="page.php?w=Terminal_alkene">terminal olefins</a>.  High-order olefins are insoluble in water, but Clement and Selwitz found that aqueous <a href="page.php?w=Dimethylformamide">DMF</a></p><p>
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