Stereoselective binding of copper(II), zinc(II), cobalt(II), and ni(II) to the optically active amino acids β-(2-pyridyl)-α-alanine and β-(6-methyl-2-pyridyl)-α-alanine, analogs of histidine and phenylalanine
Author:
Publisher
Elsevier BV
Subject
Biochemistry,General Medicine
Reference34 articles.
1. The isomers of complexes of α-amino-acids with copper(II)
2. Stability constants of copper(II) complexes of optically active α-amino-acids
3. Stability constants of nickel (II), cobalt (II) and copper (II) complexes of some optically active and racemic amino-acids
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1. σ-Pyridine Coordination Compounds with Transition Metals;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
2. Potentiometric and spectroscopic studies on copper(II) complexes of non-proteinogenic histidine analogues;Polyhedron;2005-05
3. Structure and Highly Stereoselective Formation of 1:2 Metal-to-Ligand complexes with triamine 2,6-bis(pyrolidin-2-yl)pyridine.meso-[2,6-bis(pyrrolidin-2yl)pyridine]nickel(II) (meso-[Ni(bpp)2]2+), a Metal Complex withS4 Symmetry;Helvetica Chimica Acta;1993-02-10
4. Transition-metal-assisted asymmetric synthesis of amino acid analogs. A new synthesis of optically pure D- and L-pyridylalanines;The Journal of Organic Chemistry;1991-03
5. Bibliography;Critical Stability Constants;1982
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