Gubala, V., Betancourt, J.E., Rivera, J.M. (2004) Expanding the hoogsteen edge of 2'-deoxyguanosine: Consequences for G-quadruplex formation. Organic Letters, 6 (25). pp. 4735-4738. ISSN 1523-7060. (doi:10.1021/ol048013v) (KAR id:45250)
PDF
Author's Accepted Manuscript
Language: English |
|
Download this file (PDF/186kB) |
|
Request a format suitable for use with assistive technology e.g. a screenreader | |
Official URL: http://dx.doi.org/10.1021/ol048013v |
Abstract
(Chemical Equation Presented) The synthesis and self-assembling properties of 8-aryl-2'-deoxyguanosine derivatives are described. Our studies suggest that a properly placed acetyl group can increase the stability and specificity of the resulting G-quadruplex supramolecules by enhancing noncovalent interactions such as hydrogen bonds and Ï?-stacking.
Item Type: | Article |
---|---|
DOI/Identification number: | 10.1021/ol048013v |
Additional information: | Unmapped bibliographic data: LA - English [Field not mapped to EPrints] J2 - Org. Lett. [Field not mapped to EPrints] C2 - 15575673 [Field not mapped to EPrints] AD - Department of Chemistry, University of Puerto Rico, RÃo Piedras Campus, RÃo Piedras, 00931, Puerto Rico [Field not mapped to EPrints] DB - Scopus [Field not mapped to EPrints] |
Uncontrolled keywords: | acetic acid derivative, deoxyguanosine, article, chemical interaction, chemical structure, hydrogen bond, synthesis, Deoxyguanosine, Hydrogen Bonding, Nucleic Acid Conformation, Solutions, Temperature |
Divisions: | Divisions > Division of Natural Sciences > Medway School of Pharmacy |
Depositing User: | Vladimir Gubala |
Date Deposited: | 14 Dec 2017 21:45 UTC |
Last Modified: | 05 Nov 2024 10:29 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/45250 (The current URI for this page, for reference purposes) |
- Link to SensusAccess
- Export to:
- RefWorks
- EPrints3 XML
- BibTeX
- CSV
- Depositors only (login required):