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|Title:||Comparative x-ray single crystal study of acetylated-β-D-galactopyranosyls azide and isothiocyanat||Authors:||Selkti, Mohamed
De Rango, Colette
|Affiliations:||Department of Chemistry||Issue Date:||1999||Part of:||Journal of carbohydrate chemistry||Volume:||18||Issue:||8||Start page:||1019||End page:||1032||Abstract:||
The structures of two peracetylated p-D-galactopyranosides substituted at theanomeric C atom with either an isothiocyanate or an azide group, have been determinedby single crystal X-ray diffraction analysis. The two compounds show very similarmolecular conformation, except for the substituent groups at the anomeric C atom andfor the acetyl groups of the 06 atoms. They crystallize in different infinite chain-typestructures. While the isothiocyanate group extends in a large intermolecular space, theazide group is placed in a more crowded environment.
|URI:||https://scholarhub.balamand.edu.lb/handle/uob/1766||DOI:||10.1080/07328309908544051||Ezproxy URL:||Link to full text||Type:||Journal Article|
|Appears in Collections:||Department of Chemistry|
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