282107-58-8

Upstream product

• 282107-55-5 8-methoxycarbonyloctyl 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 
• 3282-30-2 pivaloyl chloride 
• 100-39-0 benzyl bromide 
• 282107-56-6 ethyl 3-O-benzyl-1-thio-α-D-arabinofuranoside 
• 282107-51-1 Ethyl 2-O-benzoyl-3-O-benzyl-1-thio-α-D-arabinofuranoside 
• 282107-54-4 8-methoxycarbonyloctyl 3-O-benzyl-α-D-arabinofuranoside 
• 282107-64-6 ethyl 3-O-benzyl-5-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside 
• 310880-65-0 ethyl 2-O-benzoyl-3-O-benzyl-5-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside 

Downstream Products

• 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 
• 282107-60-2 8-(methoxycarbonyl)octyl 2-O-(2-O-acetyl-3-O-benzyl)-β-D-arabinofuranosyl)-3-O-benzyl-5-O-pivaloyl-α-D-arabinofuranoside 
• 628686-53-3 9-[(2S,3S,4R,5R)-3-[(2S,3S,4R,5R)-3-Acetoxy-4-benzyloxy-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-2-yloxy]-4-benzyloxy-5-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-furan-2-yloxy]-nonanoic acid methyl ester 

Relevant academic research and scientific papers

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.