899435-85-9

Upstream product

• 53403-35-3 1-O-Acetyl-2,3,5-tri-O-benzoyl-α-D-arabinofuranose 
• 899435-83-7 C₅₄H₅₈O₈ 
• 899435-82-6 C₅₄H₅₆O₈ 
• 899435-78-0 C₂₉H₂₆O₇ 
• 899435-79-1 C₂₉H₂₆O₇ 
• 899435-81-5 (2R,3R,4R,5R)-3,4-Bis-benzyloxy-2-benzyloxymethyl-5-((E)-propenyl)-tetrahydro-furan 
• 899435-80-4 (2R,3S,4S,5R)-2-Hydroxymethyl-5-((E)-propenyl)-tetrahydro-furan-3,4-diol 
• 899435-84-8 {(2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-[2-((2R,3R,4R,5R)-3,4-bis-benzyloxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-ethyl]-tetrahydro-furan-2-yl}-methanol 
• 76-83-5 trityl chloride 

Downstream Products

• 899435-87-1 {(2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-[2-((2R,3R,4R,5R)-3,4-bis-benzyloxy-5-octyloxymethyl-tetrahydro-furan-2-yl)-ethyl]-tetrahydro-furan-2-yl}-methanol 

Relevant academic research and scientific papers

An olefin cross metathesis approach to C-disaccharide analogs of the α-d-arabinofuranosyl-(1→5)-α-d-arabinofuranoside motif found in the mycobacterial cell wall

Reported is the synthesis of a C-disaccharide analog of the α-d-Araf-(1→5)-α-d-Araf motif present in the cell wall of mycobacteria, including the human pathogen Mycobacterium tuberculosis. The key step is an olefin cross metathesis reaction that proceeds