126380-65-2

Upstream product

• 21085-72-3 1-bromo-2,3,4-tri-O-acetyl-α-D-glucuronic acid methyl ester 
• 126380-63-0 (2S,3S,4S,5R,6R)-3,4,5-Tris-allyloxycarbonyloxy-6-(3,4-dimethoxy-benzyloxy)-tetrahydro-pyran-2-carboxylic acid benzyl ester 
• 126380-62-9 (2S,3S,4S,5R,6R)-3,4,5-Tris-allyloxycarbonyloxy-6-(3,4-dimethoxy-benzyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 126380-58-3 (2S,3S,4S,5R)-3,4,5-Tris-allyloxycarbonyloxy-6-hydroxy-tetrahydro-pyran-2-carboxylic acid benzyl ester 
• 126380-61-8 (2S,3S,4S,5R,6R)-6-(3,4-Dimethoxy-benzyloxy)-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 50621-74-4 (2S,3S,4S,5R,6R)-3,4,5-Triacetoxy-6-(3,4-dimethoxy-benzyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 126380-64-1 (2S,3S,4S,5R,6S)-3,4,5-Tris-allyloxycarbonyloxy-6-(5-benzoyl-6-hydroxy-indane-1-carbonyloxy)-tetrahydro-pyran-2-carboxylic acid benzyl ester 

Downstream Products

• 126380-66-3 (2S,3S,4S,5R,6S)-6-(5-Benzoyl-6-hydroxy-indane-1-carbonyloxy)-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid 

Relevant academic research and scientific papers

A NEW PROTECTED FORM OF GLUCURONIC ACID FOR THE SYNTHESIS OF LABILE 1-O-ACYL-β-D-GLUCURONIDES

A new approach to functionalized 1-O-acyl-β-D-glucuronides is described.An essential element of this strategy is the use of the easily removable allyloxycarbonyl group for the protection of the hydroxylic functions of glucuronic acid.