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) (KAR id:45249)

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Official URL: http://dx.doi.org/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, RÃo 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:	Divisions > Division of Natural Sciences > Medway School of Pharmacy
Depositing User:	Vladimir Gubala
Date Deposited:	14 Dec 2017 21:40 UTC
Last Modified:	05 Nov 2024 10:29 UTC
Resource URI:	https://kar.kent.ac.uk/id/eprint/45249 (The current URI for this page, for reference purposes)

University of Kent Author Information

Gubala, V..

Creator's ORCID:	https://orcid.org/0000-0001-6301-3632
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