Issue 38, 2011
From the journal:

Dalton Transactions

Coordination chemistry and biological activity of 5′-OH modified quinoline–B12 derivatives†

Karel Zelenka,a   Helmut Brandl,b   Bernhard Spinglera  and  Felix Zelder*a  

* Corresponding authors

a Institute of Inorganic Chemistry, University of Zürich, Winterthurerstr. 190, Zürich, Switzerland
E-mail: zelder@aci.uzh.ch,http://www.zelder.ch.vu
Fax: +41 44 63 56802
Tel: +41 44 63 54624

b Institute of Evolutionary Biology and Environmental Studies, University of Zürich, Winterthurerstrasse 190, Zürich, Switzerland

Abstract

The consequences of structural modifications at the 5′-OH ribofuranotide moiety of quinoline modified B12 derivatives are discussed in regard of the coordination chemistry, the electrochemical properties and the biological behaviour of the compound.

Graphical abstract: Coordination chemistry and biological activity of 5′-OH modified quinoline–B12 derivatives

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Article information

DOI
https://doi.org/10.1039/C1DT11161B
Article type
Communication
Submitted
20 Jun 2011
Accepted
27 Jul 2011
First published
18 Aug 2011

Dalton Trans., 2011,40, 9665-9667

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Coordination chemistry and biological activity of 5′-OH modified quinoline–B12 derivatives

K. Zelenka, H. Brandl, B. Spingler and F. Zelder, Dalton Trans., 2011, 40, 9665 DOI: 10.1039/C1DT11161B

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