Pregled bibliografske jedinice broj: 152170
Stereochemical Assignment of Diastereomeric Imidazolidinone Ring Containing Bicyclic Sugar-peptide Adducts: NMR Spectroscopy and Molecular Calculations
Stereochemical Assignment of Diastereomeric Imidazolidinone Ring Containing Bicyclic Sugar-peptide Adducts: NMR Spectroscopy and Molecular Calculations // European journal of organic chemistry, (2004), 4641-4647 (međunarodna recenzija, članak, znanstveni)
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Naslov
Stereochemical Assignment of Diastereomeric Imidazolidinone Ring Containing Bicyclic Sugar-peptide Adducts: NMR Spectroscopy and Molecular Calculations
Autori
Roščić, Maja ; Eklund, Robert ; Nordmark, Eva-Lisa ; Horvat, Štefica ; Widmalm, Goran
Izvornik
European journal of organic chemistry (1434-193X)
(2004);
4641-4647
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Carbohydrates; Imidazolidinone; Leu-enkephalin; Conformation; NMR spectroscopy; Molecular calculations
Sažetak
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.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
Uključenost u ostale bibliografske baze podataka::
- Chemical Abstracts
