75671-00-0

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 124-63-0 methanesulfonyl chloride 
• 17791-36-5 methyl 2,3-di-O-benzyl-α-D-glucopyranoside 
• 111727-15-2 (2R,3R,4S,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-ol 
• 3162-96-7 methyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 7177-79-9 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 

Downstream Products

• 116013-34-4 (2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate 
• 116013-32-2 Methyl 2,3-di-O-benzyl-4-deoxy-6-aldehydo-β-L-threo-hex-4-enodialdo-1,5-pyranoside 
• 75670-98-3 methyl 2,3-di-O-benzyl-4-deoxy-4-fluoro-α-D-galactopyranoside 

Relevant academic research and scientific papers

Linearization of carbohydrate derived polycyclic frameworks

We report easy access to carbohydrate derived diverse tricyclic skeletons which could be beneficial for exploring polyfunctionalized chiral alicycles. The key reaction to assemble a sugar fused tricyclic core is intermolecular tandem esterification and 1,3-dipolar cycloaddition. The framework was elaborated using amide forming reactions, opening of isoxazolidine rings followed by N and O-acylations. The sequences provide distinct, spatially separated and encoded chemical entities that may pave the way to investigate cell functions.

Specificity of α- and β-D-galactosidase towards analogs of D-galactopyranosides modified at C-4 or C-5

In examining the stereochemistry of D-galactose oxidase, it was found that some 4-deoxy analogs of methyl β-D-galactopyranoside (1), particularly the 4-amino (2) and 4-fluoro (3) derivatives, are relatively good substrates of the enzyme.The same compounds