DNA duplexes stabilized by modified monomer residues: synthesis and stability

Tools

Graham, Duncan and Parkinson, John A. and Brown, Tom (1998) DNA duplexes stabilized by modified monomer residues: synthesis and stability. Journal of the Chemical Society, Perkin Transactions 1, 1998 (6). pp. 1131-1138. ISSN 1472-7781 (http://dx.doi.org/10.1039/a707031d)

Full text not available in this repository.Request a copy

Abstract

The synthesis of a series of 2'-deoxyuridine analogues modified at the 5-position and a series of 2'-deoxypurines modified at the 8-position is described. Ultraviolet melting studies have been used to assess the stability of DNA duplexes 12- and 8-residues in length that contain these modifications. Of those modified residues which have been incorporated into oligonucleotides, 5-(prop-1-ynyl)-2'-deoxyuridine is found to impart the greatest increase in stability on the DNA duplexes studied.

ORCID iDs

Graham, Duncan ORCID logoORCID: https://orcid.org/0000-0002-6079-2105, Parkinson, John A. ORCID logoORCID: https://orcid.org/0000-0003-4270-6135 and Brown, Tom;
CORE (COnnecting REpositories)