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Inside Cover: Stereoselective Formation of Chiral Metallopeptides (Chem. Eur. J. 23/2012)
Author(s) -
Rama Gustavo,
Ardá Ana,
Maréchal JeanDidier,
Gamba Ilaria,
Ishida Hitoshi,
JiménezBarbero Jesús,
Vázquez M. Eugenio,
Vázquez López Miguel
Publication year - 2012
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201290093
Subject(s) - chirality (physics) , stereochemistry , cover (algebra) , stereoselectivity , proline , chemistry , ligand (biochemistry) , amino acid , physics , receptor , biochemistry , chiral symmetry , engineering , catalysis , quantum mechanics , nambu–jona lasinio model , quark , mechanical engineering
Ligand effects The chirality of a metallopeptide is determined by the chirality of a single proline amino acid ( D ‐ or L ‐ P) located between the two coordinating 2,2′‐bipyridine residues. In their Communication on page 7030 ff. , M. Vázquez López, J. Jiménez‐Barbero, M. E. Vázquez et al. describe the synthesis as well as the structural elucidation of the complexes.