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In organic chemistry, the hydroboration-oxidation reaction is a two-step hydration reaction that converts an alkene into an alcohol.[1] The process results in the syn addition of a hydrogen and a hydroxyl group where the double bond had been. Hydroboration-oxidation is an anti-Markovnikovreaction, with the hydroxyl group attaching to the less-substituted carbon. The reaction thus provides a more stereospecific and complementary regiochemical alternative to other hydration reactions such as acid-catalyzed addition and the oxymercuration-reduction process.
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