The tertiary alcohol is then subjected to a reaction with a diol, typically in the presence of an acid catalyst. This forms a cyclic acetal, resulting in the formation of the 2-R-1,3-dioxane ring.
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4-(1,3-dioxan-2-yl)-2-ethoxyphenyl propanoate
1-[bis(n-butylthio)methyl]-4-chlorobenzene
phenyl 6-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside
