Chiral pyridine-type ligands are readily available in enantiomerically pure
form from enantiopure natural products via a Krohnke reaction. The ease of
synthesis allows numerous variations of the ligands which all display a pa
rticular coordination behavior. By these means, it is possible to synthesiz
e 'tunable' series of molecules. Thus, mononuclear, as well as self-assembl
ed polynuclear species can be obtained in enantiopure form. With these liga
nds, a significant step towards the systematic development of stereoselecti
ve synthesis in coordination chemistry was achieved, leading to a class of
compounds that hold interest for various kinds of applications.