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Updated: Aug 2, 2026

Analyzing and Building Nucleic Acid Structures with 3DNA
Published on: April 26, 2013
Synthesis of 5-substituted [N3-15N]-pyrimidine nucleosides: Developing model systems for NMR studies of substituent
1Department of Chemistry, CREST, Graduate School of Science, Tokyo Metropolitan University, Tokyo, Japan.
Abstract:
The effects on various NMR parameters of substitutions, which may influence the hydrogen bond strengths of Watson-Crick-type base pairs, were investigated for DNA dodecamers containing 5-substituted-2'-deoxyuridine derivatives in oligomers, 5'-d(CGCGAATXCGCG)-3', where A and X were [ul-15N]-2'-deoxyadenosine and [3(-15)N]-2'-deoxyuridine derivatives. The substitution effects on the NMR parameters were linearly correlated with the pKa values of the 2'-deoxyuridine derivatives.
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