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Updated: Apr 5, 2026

Chemical Triphosphorylation of Oligonucleotides
Published on: June 2, 2022
Direct synthesis of methyl phosphoramidates in carbohydrates
Vijay M Dhurandhare1, Girija Prasad Mishra, Sarah Lam
1Institute of Chemistry, Academia Sinica, 128, Section 2, Academia Road, Taipei 115, Taiwan. wangcc@chem.sinica.edu.tw.
Abstract:
A direct installation of a methyl phosphoramidate group by using methyl benzylphosphoramidochloridate into carbohydrates and amino acid is described. This one-step synthesis is efficient for both primary and secondary alcohols and exhibited excellent regioselectivity and functional group compatibility. Formation of a single diastereomer is observed in certain cases. The N-benzyl protecting group on methyl phosphoramidates is easily removed under mild conditions.
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