146897-32-7

Upstream product

• 72886-95-4 Methyl-5-O-benzyl-1,3-O-benzyliden-β-D-fructopyranosid 
• 5123-94-4 5-Benzyl-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 18610-08-7 Methyl-1,3-O-benzyliden-4-O-mesyl-β-D-fructopyranosid 
• 77387-17-8 Methyl-5-O-benzyl-1,3-O-benzyliden-β-D-threo-hexo-2,4-diulo-pyranosid 
• 77387-07-6 Methyl-5-O-benzyl-1,3-O-benzyliden-4-O-mesyl-β-D-fructopyranosid 
• 72886-94-3 Methyl-5-O-benzyl-1,3-O-benzyliden-α-L-sorbopyranosid 
• 18610-08-7 Methyl-1,3-O-benzyliden-4-O-mesyl-α-L-sorbopyranosid 
• 77387-17-8 Methyl-5-O-benzyl-1,3-O-benzyliden-α-L-erythro-hexo-2,4-diulo-pyranosid 
• 77387-07-6 Methyl-5-O-benzyl-1,3-O-benzyliden-4-O-mesyl-α-L-sorbopyranosid 
• 72886-92-1 Methyl-5-O-benzyl-1,3-O-benzyliden-β-D-tagatopyranosid 
• 77387-10-1 Methyl-4-O-acetyl-5-O-benzyl-1,3-O-benzyliden-α-L-psicopyranosid 
• 72886-93-2 Methyl-5-O-benzyl-1,3-O-benzyliden-α-L-psicopyranosid 

Relevant academic research and scientific papers

A novel synthetic application of glucose isomerase: Quantitative conversion of D-glucose and L-idofuranose, derivatives modified at position five into the corresponding D-fructo- and L-sorbopyranoses

Glucose isomerase (B.C. 5.3.1.5) quantitatively converts a wide range of D-glucose as well as L-idose derivatives modified at position five, such as 5-O-benzyl-, 5-azido-5-deoxy-, 5-deoxy-5-fluoro analogues into the corresponding 2-ketosugars. The reactio

Synthesis of 5- and 6-O-Alkyl substituted Ketohexoses of the L-sorbo-, L-psico-, D-fructo-, and D-tagato-Series

Starting from methyl 1,3-O-benzyliden-β-D-fructopyranoside 1 the synthesis of 5-O-benzyl-D-fructose 9 and, after inversion of the configuration at C-4 by oxydation and subsequent stereoselective reduction, the synthesis of 5-O-benzyl- and 5-O-methyl-D-tag