628686-53-3

Upstream product

• 108-24-7 acetic anhydride 
• 282107-59-9 8-(methoxycarbonyl)octyl 2-O-(3-O-benzyl-5-O-tert-butyldiphenylsilyl)-β-D-arabinofuranosyl)-3-O-benzyl-5-O-pivaloyl-α-D-arabinofuranoside 
• 282107-57-7 ethyl 3-O-benzyl-5-O-tert-butyldiphenylsilyl-2-O-(4-methoxybenzyl)-1-thio-α-D-arabinofuranoside 
• 34957-73-8 methyl 9-hydroxynonanoate 
• 282107-58-8 9-[4-benzyloxy-3-[[4-benzyloxy-5-(tert-butyl-diphenyl-silanyloxymethyl)-2-ethylsulfanyl-tetrahydro-furan-3-yloxy]-(4-methoxy-phenyl)-methoxy]-5-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-furan-2-yloxy]-nonanoic acid methyl ester 
• 310880-65-0 ethyl 2-O-benzoyl-3-O-benzyl-5-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside 
• 282107-64-6 ethyl 3-O-benzyl-5-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside 
• 282107-54-4 8-methoxycarbonyloctyl 3-O-benzyl-α-D-arabinofuranoside 
• 282107-51-1 Ethyl 2-O-benzoyl-3-O-benzyl-1-thio-α-D-arabinofuranoside 
• 282107-56-6 ethyl 3-O-benzyl-1-thio-α-D-arabinofuranoside 
• 100-39-0 benzyl bromide 
• 3282-30-2 pivaloyl chloride 

Downstream Products

• 282107-60-2 8-(methoxycarbonyl)octyl 2-O-(2-O-acetyl-3-O-benzyl)-β-D-arabinofuranosyl)-3-O-benzyl-5-O-pivaloyl-α-D-arabinofuranoside 

Relevant academic research and scientific papers

Synthesis of oligoarabinofuranosides from the mycobacterial cell wall

Oligoarabinofuranosides 1-4, fragments of the arabinan components found in the mycobacterial cell wall have been synthesized. 1 and 2 are representative of the structural features of the internal core of arabinogalactan, arabinomannan and lipoarabinomanna

1,2,5-Ortho esters of D-arabinose as versatile arabinofuranosidic building blocks. Concise synthesis of the tetrasaccharidic cap of the lipoarabinomannan of Mycobacterium tuberculosis

1,2,5-ortho esters of D-arabinose were found to be ideally suited building blocks for the stereoselective formation of and β arabinofuranosidic linkages after nucleophilic opening of the orthoester with oxygen and sulfur nucleophiles; the tetrasaccharidic cap of the lipoarabinomannan of Mycobacterium tuberculosis was then synthesized in a highly convergent manner.