237410-28-5

Upstream product

• 67-56-1 methanol 
• 14645-49-9 methyl 2,3-anhydro-5-O-benzyl-α-D-lyxofuranoside 
• 56607-40-0 methyl D-arabinofuranoside 
• 1427519-51-4 methyl 2,3-di-O-methoxybenzyl-5-O-benzyl-α-D-arabinofuranoside 
• 1186016-51-2 methyl 2,3-di-O-(4-methoxybenzyl)-α-D-arabinofuranoside 
• 1186016-52-3 methyl 2,3-di-O-(4-methoxybenzyl)-5-O-(tert-butyldiphenylsilyl)-α-D-arabinofuranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 329360-22-7 1-O-methyl-3,5-di-O-benzyl-α-D-arabinofuranose 
• 527681-69-2 methyl 2-O-(5-O-benzoyl-2-deoxy-2-p-thiotolyl-β-D-xylofuranosyl)-3,5-di-O-benzyl-α-D-arabinofuranoside 
• 14645-49-9 methyl 2,3-anhydro-5-O-benzyl-α-D-lyxofuranoside 

Relevant academic research and scientific papers

Design, synthesis and activity of thio-linked arabinofuranosyl disaccharides against mycobacterial tuberculosis (MTB) and Mycobacterium avium complex (MAC)

We report the chemical synthesis of a series of disaccharides of arabinofuranose with a glycosidic sulfur linker as mimics of the acceptor for arabinofuranosyltransferases with and without using any activator to avoid any complex reactions. These analogs were tested for in vitro activity against MTB strain H37Ra and 3 MAC clinical isolates. MICs were determined using a colorimetric microdilution broth assay. Bactericidal activity was studied with kill curves over a period of seven days. Intracellular activity against MTB H37Ra was determined in the Mono Mac 6 (MM6) human monocytic cell line. ARKAT-USA, Inc.

A novel route for the synthesis of deoxy fluoro sugars and nucleosides

The reaction of (diethylamino)sulfur trifluoride (DAST) with methyl 5-O- benzoyl-β-D-xylofuranoside (1) followed by column chromatography afforded the riboside 2 (62%) and the ribo-epoxide 3 (18%) (Scheme 1). Under similar reaction conditions, the α-D-ano