Efficient isomerization of methyl arabinofuranosides into corresponding arabinopyranosides in presence of pyridine
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文摘

Selective synthesis of methyl β-D-arabinopyranoside from arabinose is described with pyridine as promotor of glycosylation.

Kinetics of the reaction is described as well as a putative mechanism where pyridine acts as a nucleophile.

Extension to other pentoses, lyxose, xylose and ribose was performed with good yields and selectivity.

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