Computing and Library Services - delivering an inspiring information environment

The mechanism of the phosphoramidite synthesis of polynucleotides

Russell, Mark A., Laws, Andrew P., Atherton, John H. and Page, Michael I. (2008) The mechanism of the phosphoramidite synthesis of polynucleotides. Organic and Biomolecular Chemistry, 6 (18). pp. 3270-3275. ISSN 1477-0539

Metadata only available from this repository.


The mechanism of the coupling step in polynucleotide synthesis using 5-4,4-dimethoxytritylthymidine-3-β-cyanoethyl-N,N-diisopropylphosphoramidite as the phosphitylating agent and catalysed by the salt of saccharin and N-methylimidazole in acetonitrile has been studied by 31P NMR. Pre- and post-equilibria between the activator salt and released diisopropylamine have been examined by 1H NMR and ITC, which show that the salt between saccharin and diisopropylamine will be present in acetonitrile. Activation of the phosphoramidite by the salt of saccharin and N-methylimidazole involves nucleophilic catalysis and the formation of a reactive saccharin adduct bonded through its carbonyl oxygen to phosphorus. The rate constants for the reaction of the 4-methoxyphenol with 5-4,4-dimethoxytritylthymidine-3-β-cyanoethyl-N,N-diisopropylphosphoramidite in the presence of saccharin–N-methylimidazole salt show a non-linear dependence on phenol concentration, becoming independent at high phenol concentrations, compatible with a change in rate limiting step from the alcoholysis step to the activation step.

Item Type: Article
Subjects: Q Science > Q Science (General)
Q Science > QD Chemistry
Schools: School of Applied Sciences
School of Applied Sciences > Biomolecular Sciences Research Centre
Related URLs:
Depositing User: Graham Stone
Date Deposited: 13 Feb 2009 13:52
Last Modified: 28 Aug 2021 10:44


Downloads per month over past year

Repository Staff Only: item control page

View Item View Item

University of Huddersfield, Queensgate, Huddersfield, HD1 3DH Copyright and Disclaimer All rights reserved ©