32780-15-7

Upstream product

• 63029-07-2 methyl 2,3-O-isopropylidene-α-D-lyxofuranoside 
• 100-44-7 benzyl chloride 

Downstream Products

• 79083-30-0 methyl 5-O-benzyl-α-D-lyxofuranoside 
• 79063-92-6 Acetic acid (1R,2S,3R)-3-acetoxy-2,4-bis-benzyloxy-1-(1-methoxy-ethyl)-butyl ester 
• 79083-31-1 methyl 5-O-benzyl-β-D-lyxofuranoside 
• 79063-93-7 (2R,3S,4S)-1-Benzyloxy-5-methoxy-hexane-2,3,4-triol 
• 79063-91-5 (2R,3S,4R)-1,3-Bis-benzyloxy-5-methoxy-hexane-2,4-diol 
• 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 

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