Title of article :
Mechanism of the transition-metal-catalyzed mutarotation reaction of N-(p-chlorophenyl)-β-d-glucopyranosylamine in methanol Original Research Article
Author/Authors :
Kazimiera Smiataczowa، نويسنده , , Jaros?aw Kosmalski، نويسنده , , Teresa Widernik، نويسنده , , Zygmunt Warnke، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2003
Pages :
7
From page :
969
To page :
975
Abstract :
Rate constants for the mutarotation reaction of N-(p-chlorophenyl)-β-d-glucopyranosylamine (NGlc) in methanol have been determined in the presence of transition metal chlorides (MCl2), at 25 °C. The activity of the metal ions catalyzing the α-pyranoside↔β-pyranoside interconversion has been found to increase in the following series: Mn2+
Keywords :
N-(p-Chlorophenyl)-?-d-glucopyranosylamine , Methanol , Metal chlorides
Journal title :
Carbohydrate Research
Serial Year :
2003
Journal title :
Carbohydrate Research
Record number :
963725
Link To Document :
