58109-23-2

Upstream product

• 58109-21-0 methyl 5,6-O-cyclohexylidene-3-deoxy-2-C-methyl-β-D-ribohexofuranoside 

Downstream Products

• 67689-95-6 (2S,3R,5S)-5-[1-Hydroxy-2-(1-methyl-cyclohexyloxy)-ethyl]-2-methoxy-3-methyl-tetrahydro-furan-3-ol 
• 67689-95-6 (2R,3R,5S)-5-[1-Hydroxy-2-(1-methyl-cyclohexyloxy)-ethyl]-2-methoxy-3-methyl-tetrahydro-furan-3-ol 
• 58109-21-0 methyl 5,6-O-cyclohexylidene-3-deoxy-2-C-methyl-α-D-ribohexofuranoside 
• 67689-95-6 (3R,5S)-5-[1-Hydroxy-2-(1-methyl-cyclohexyloxy)-ethyl]-2-methoxy-3-methyl-tetrahydro-furan-3-ol 
• 67689-95-6 (3S,5S)-5-[1-Hydroxy-2-(1-methyl-cyclohexyloxy)-ethyl]-2-methoxy-3-methyl-tetrahydro-furan-3-ol 
• 6236-09-5 (S)-citramalic acid 

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