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Mechanism of the transition-metal-catalyzed mutarotation reaction of N-(p-chlorophenyl)-beta-D-glucopyranosylamine in methanol
Authors:Smiataczowa Kazimiera  Kosmalski Jarosław  Widernik Teresa  Warnke Zygmunt
Affiliation:Faculty of Chemistry, University of Gdańsk, Sobieskiego 18, PL-80-952 Gdańsk, Poland.
Abstract:Rate constants for the mutarotation reaction of N-(p-chlorophenyl)-beta-D-glucopyranosylamine (NGlc) in methanol have been determined in the presence of transition metal chlorides (MCl(2)), at 25 degrees C. The activity of the metal ions catalyzing the alpha-pyranoside<-->beta-pyranoside interconversion has been found to increase in the following series: Mn(2+)
Keywords:N-(p-Chlorophenyl)-β-  smallcaps"  >d-glucopyranosylamine   Methanol   Metal chlorides
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