548477-88-9

Upstream product

• 220608-60-6 (2S,3S,4S,5R,6R)-3,4,5-Tris-benzoyloxy-6-benzyloxy-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 98-88-4 benzoyl chloride 
• 87924-24-1 benzyl 2,3,4-tri-O-benzoyl-β-D-glucopyranoside 
• 291528-10-4 benzyl 6-O-tert-butyldiphenylsilyl-β-D-glucopyranoside 
• 220608-55-9 C₅₀H₄₈O₉Si 
• 4304-12-5 (2R,3R,4S,5S,6R)-2-(benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 
• 103674-69-7 methyl 2,3,4-tri-O-benzoyl-1-bromo-1-deoxy-α-D-glucopyranuronate 
• 82228-14-6 methyl D-glucopyranuronate 
• 150608-11-0 methyl 1,2,3,4-tetra-O-benzoyl-β-D-glucopyranuronate 

Downstream Products

• 169557-99-7 2,3,4-tri-O-benzoyl-1-deoxy-1-(2,2,2-trichloro-1-iminoethoxy)-α-D-glucopyranuronate, methyl ester 

Relevant academic research and scientific papers

Synthesis of glucuronic acid derivatives via the efficient and selective removal of a C6 methyl group

This investigation is related to the development of a general strategy for the synthesis of certain glucuronic acid derivatives. In particular, we report exceptionally selective conditions for removing the C6 methyl protecting group by potassium hydroxide