These are highly reactive intermediates that result from the protonation of the anomeric carbon. They can be trapped using nucleophiles like methanol or water to form stable products. By analyzing the structures of these trapped intermediates, researchers can gain insights into the reaction mechanism.
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methyl 3,6-di-O-benzyl-2-deoxy-α-D-arabino-hexopyranoside
3-(p-methoxyphenyl)propanal dimethylacetal
tris(benzyloxymethyl)carbinol
