Skip to main content

Self-assembled ionophores based on 8-phenyl-2'-deoxyguanosine analogues

Gubala, V., De Jesus, D., Rivera, J.M. (2006) Self-assembled ionophores based on 8-phenyl-2'-deoxyguanosine analogues. Tetrahedron Letters, 47 (9). pp. 1413-1416. ISSN 0040-4039. (doi:10.1016/j.tetlet.2005.12.100)

Abstract

Novel base-modified G-analogues act as self-assembled ionophores for various metal cations. Their extracting efficiency can be modulated by the presence and substitution pattern of a functionalized phenyl group that replaces the H8 in the guanine base.

Item Type: Article
DOI/Identification number: 10.1016/j.tetlet.2005.12.100
Additional information: Unmapped bibliographic data: LA - English [Field not mapped to EPrints] J2 - Tetrahedron Lett. [Field not mapped to EPrints] AD - Department of Chemistry, University of Puerto Rico, Río Piedras Campus, San Juan 00931, Puerto Rico [Field not mapped to EPrints] DB - Scopus [Field not mapped to EPrints]
Uncontrolled keywords: G-analogues, G-quadruplex, Ionophores, Self-assembly, 8 phenyl 2' deoxyguanosine, guanine, guanosine derivative, ionophore, metal ion, phenyl group, unclassified drug, article, extraction, molecular model, nuclear magnetic resonance spectroscopy
Divisions: Faculties > Sciences > Medway School of Pharmacy
Depositing User: Vladimir Gubala
Date Deposited: 14 Dec 2017 21:40 UTC
Last Modified: 29 May 2019 13:42 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/45249 (The current URI for this page, for reference purposes)
Gubala, V.: https://orcid.org/0000-0001-6301-3632
  • Depositors only (login required):

Downloads

Downloads per month over past year