148260-64-4

Upstream product

• 148180-43-2 2,3,6-Tri-O-benzoyl-4'-O-trifluoromethylsulfonyl-α-D-glucopyranosyl 2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside 
• 61207-38-3 2,3,6-Tri-O-benzoyl-α-D-glucopyranosyl 2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside 

Downstream Products

• 51855-99-3 4-amino-4-deoxy-α-D-glucopyranosyl α-D-glucopyranoside 
• 148180-46-5 2,3,6-Tri-O-benzoyl-4-deoxy-4-trifluoroacetamido-α-D-glucopyranosyl 2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Probing the mycobacterial trehalome with bioorthogonal chemistry

Mycobacteria, including the pathogen Mycobacterium tuberculosis, use the non-mammalian disaccharide trehalose as a precursor for essential cell-wall glycolipids and other metabolites. Here we describe a strategy for exploiting trehalose metabolic pathways

An improved synthesis of 4-azido-4-deoxy- and 4-amino-4-deoxy-α,α-trehalose and their epimers

The order of esterification of the eight hydroxyl groups of α,α-trehalose is HO-6,6' > HO-2,2' > HO-3,3' > HO-4,4'.Under the appropriate conditions of benzoylation, the heptabenzoate with HO-4' free was obtained in good yield (58percent), along with the o