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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

Roščić, Maja ; Eklund, Robert ; Nordmark, Eva-Lisa ; Horvat, Štefica ; Widmalm, Goran Stereochemical Assignment of Diastereomeric Imidazolidinone Ring Containing Bicyclic Sugar-peptide Adducts: NMR Spectroscopy and Molecular Calculations // European journal of organic chemistry, (2004), 4641-4647-x

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

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Podaci o izdanju

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2004.

4641-4647-x

objavljeno

1434-193X

Povezanost rada

Kemija

Indeksiranost