Abstract
AbstractAddition of protonated formaldehyde to 1‐dodecene in acetic acid solution yields 4‐decyl‐1,3‐dioxane and both cis‐ and trans‐4‐acetoxy‐3‐nonyltetrahydropyran as major products. The configuration of these reaction products was investigated by proton magnetic resonance. Their formation is explained by a recently reported reaction mechanism.
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