A method for obtaining equilibrium tautomeric mixtures of reducing sugars via glycosylamines using nonaqueous media
SS Allavudeen, B Kuberan, D Loganathan
Index: Allavudeen, Sikkander Sulthan; Kuberan, Balagurunathan; Loganathan, Duraikkannu Carbohydrate Research, 2002 , vol. 337, # 10 p. 965 - 968
Full Text: HTML
Citation Number: 10
Abstract
Equilibrium tautomeric mixtures of several mono-and disaccharides are obtained in anhydrous form, without the use of water, by reacting the commercially available reducing sugars with ammonia gas in dry methanol, followed by the concentration of the resultant solution to dryness. Mutarotation and hydrolysis of the initially formed glycosylamine in the resultant medium account for the transformation. Equilibrium anomeric mixtures enriched ...
Related Articles:
[Giese, Bernd; Gilges, Stefan; Groeninger, Kay S.; Lamberth, Clemens; Witzel, Tom Liebigs Annalen der Chemie, 1988 , p. 615 - 617]
[Bruyere, Isabelle; Toth, Zoltan; Benyahia, Hamida; Xue, Jia Lu; Praly, Jean-Pierre Tetrahedron, 2013 , vol. 69, # 46 p. 9656 - 9662]
[Praly, Jean-Pierre; Ardakani, Azin Salek; Bruyere, Isabelle; Marie-Luce, Chrystelle; Bing Qin, Bing Carbohydrate Research, 2002 , vol. 337, # 18 p. 1623 - 1632]
[Bruyere, Isabelle; Toth, Zoltan; Benyahia, Hamida; Xue, Jia Lu; Praly, Jean-Pierre Tetrahedron, 2013 , vol. 69, # 46 p. 9656 - 9662]
[Praly, Jean-Pierre; Ardakani, Azin Salek; Bruyere, Isabelle; Marie-Luce, Chrystelle; Bing Qin, Bing Carbohydrate Research, 2002 , vol. 337, # 18 p. 1623 - 1632]