Stereochemical Assignment of Diastereomeric Imidazolidinone Ring Containing Bicyclic Sugar-peptide Adducts: NMR Spectroscopy and Molecular Calculations (CROSBI ID 106407)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Roščić, Maja ; Eklund, Robert ; Nordmark, Eva-Lisa ; Horvat, Štefica ; Widmalm, Goran
engleski
Stereochemical Assignment of Diastereomeric Imidazolidinone Ring Containing Bicyclic Sugar-peptide Adducts: NMR Spectroscopy and Molecular Calculations
The combination of NMR spectroscopy and molecular simulations was used to determine trans/cis configurational features of two diastereomeric bicyclic imidazolidinone compounds obtained by intramolecular cyclization of monosaccharide ester of leucine-enkephalin related to D-glucose.
Carbohydrates; Imidazolidinone; Leu-enkephalin; Conformation; NMR spectroscopy; Molecular calculations
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano