87326-89-4

Upstream product

• 108-24-7 acetic anhydride 
• 87326-88-3 methyl 6-deoxy-6-iodo-2,3-bis-O-(phenylmethyl)-α-D-glucopyranoside 
• 17791-36-5 methyl 2,3-di-O-benzyl-α-D-glucopyranoside 

Downstream Products

• 87326-90-7 methyl 4-O-acetyl-2,3-di-O-benzyl-6-deoxy-α-D-xylo-hex-5-enopyranoside 
• 17791-36-5 methyl 2,3-di-O-benzyl-α-D-glucopyranoside 
• 87392-25-4 methyl 2,3-di-O-benzyl-β-L-idopyranoside 
• 87326-96-3 methyl uronate 
• 87907-55-9 methyl uronate 
• 87326-92-9 methyl 4-O-benzoyl-2,3-di-O-benzyl-6-O-trityl-β-L-idopyranoside 
• 87326-47-4 methyl 4-O-benzoyl-2,3-di-O-benzyl-β-L-idopyranoside 
• 87326-95-2 methyl (methyl 2,3-di-O-benzyl-β-L-idopyranosid)uronate 
• 54522-57-5 methyl-2,3-di-O-benzyl-6-O-(4-toluenesulfonyl)-α-D-glucopyranoside 
• 87326-88-3 methyl 6-deoxy-6-iodo-2,3-bis-O-(phenylmethyl)-α-D-glucopyranoside 

Relevant academic research and scientific papers

CHEMICAL SYNTHESIS OF L-IDURONIC ACID-CONTAINING DISACCHARIDIC FRAGMENTS OF HEPARIN

Condensation of methyl 3-O-benzyl-2-benzyloxycarbonylamino-6-O-chloroacetyl-2-deoxy-α-D-glucopyranoside with methyl (2,3,4-tri-O-acetyl-α-L-idopyranosyl bromide)uronate in 1,2-dichloroethane, in the presence of silver triflate and molecular sieves, provid

α-Glucosidase Inhibitors, 5.- Investigations towards a Synthesis of C1-Branched Cyclitols from D-Glucose

The glucose derivatives 1 and 2 were transformed by Ferrier rearrangement as one of the reaction steps into the cyclitol derivatives 3a,b and 4a,b, respectively.The attachment of a functional C1-side chain at the carbonyl group was tested with