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Glycosylamines. 3.  Preparation, Structure, and Conformation of Some Glycosylamines

K. Linek, J. Alföldi, and M. Ďurindová

Institute of Chemistry, Slovak Academy of Sciences, CS-842 38 Bratislava

 

Abstract: Di-β-D-galactopyranosylamine has been prepared by transglycosylation of β-D-galactopyranosylamine. By treatment of 4,6-O-ethylidene-α-D-glucopyranose with ammonia 4,6-O-ethylidene-β-D-glucopyranosylamine was prepared. The structure, anomeric configuration, and conformation of these compounds as well as of N-acetyi-β-D-glucopyranosylamine, N-acetyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranosylamine, and N-acetyl-β-D-mannopyranosylamine were determined by 1H and 13C NMR spectroscopy.

Full paper in Portable Document Format: 474a247.pdf

 

Chemical Papers 47 (4) 247–250 (1993)

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