DNA duplexes stabilized by modified monomer residues: synthesis and stability
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)
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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: https://orcid.org/0000-0002-6079-2105, Parkinson, John A. ORCID: https://orcid.org/0000-0003-4270-6135 and Brown, Tom;-
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Item type: Article ID code: 950 Dates: DateEvent21 March 1998PublishedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry Depositing user: Mr Derek Boyle Date deposited: 04 May 2006 Last modified: 11 Nov 2024 08:13 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/950