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Determination of Amino Acid Enantiopurity and Absolute Configuration: Synergism between Configurationally Labile Metal‐Based Receptors and Dynamic Covalent Interactions
Author(s) -
Scaramuzzo Francesca A.,
Licini Giulia,
Zonta Cristiano
Publication year - 2013
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201302721
Subject(s) - absolute configuration , covalent bond , chemistry , metal , receptor , stereochemistry , organic chemistry , biochemistry
Abstract Reliable determination of the enantiomeric excess of free amino acids can be obtained by measuring the induced circular dichroism of a multicomponent assembly formed by a modified tris(2‐pyridylmethyl)amine ligand, a zinc salt, and the amino acid of interest. The systems furnish reliable information for all natural amino acids.

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