79063-91-5

Upstream product

• 79083-33-3 methyl 2,3,5-tri-O-benzyl-β-D-lyxofuranosiden 
• 79083-32-2 methyl 2,3,5-tri-O-benzyl-α-D-lyxofuranosiden 
• 63029-07-2 methyl 2,3-O-isopropylidene-α-D-lyxofuranoside 
• 32780-15-7 methyl 5-O-benzyl-2,3-O-isopropylidene-α-D-lyxofuranoside 
• 100-44-7 benzyl chloride 
• 917-64-6 methyl magnesium iodide 
• 79083-39-9 1-O-methyl 3,5-di-O-benzyl β(D)xylo-pentoaldofuranose 
• 22250-06-2 1,2-O-Cyclohexylidene-α-D-xylofuranose 
• 79063-96-0 3,5-di-O-benzyl-1,2-O-cyclohexylidene-α-D-xylofuranose 
• 79083-31-1 methyl 5-O-benzyl-β-D-lyxofuranoside 
• 79083-30-0 methyl 5-O-benzyl-α-D-lyxofuranoside 

Downstream Products

• 79063-92-6 Acetic acid (1R,2S,3R)-3-acetoxy-2,4-bis-benzyloxy-1-(1-methoxy-ethyl)-butyl ester 

Relevant academic research and scientific papers

The Use of Grignard Reagents in the Synthesis of Carbohydrates. III. The One-way Anomerization of Methyl Glycofuranosides and the Opening of Their Furanose Rings

The anomerization of methyl glycofuranoside derivatives with methylmagnesium iodide or t-butylmagnesium bromide occurred in a one-way manner.For example, methyl 5-O-benzyl-β-D-ribofuranoside (3β) was converted into the corresponding α-anomer (3α) in a 95p