1431370-75-0

Upstream product

• 1449125-95-4 C₁₀H₁₈O₅ 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 1449125-96-5 C₄₀H₄₈O₅Si 
• 1431370-78-3 C₄₈H₇₀O₁₀Si₂ 
• 1431370-77-2 C₄₁H₆₄O₁₀Si₂ 
• 1431370-62-5 pent-4-enyl 2,3-di-O-benzyl-5-O-(2-O-benzyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside 
• 1431370-61-4 pent-4-enyl 2,3-di-O-benzyl-5-O-(α-D-arabinofuranosyl)-α-D-arabinofuranoside 
• 1431370-60-3 pent-4-enyl 2,3-di-O-benzyl-5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside 
• 1187620-69-4 pent-4-enyl 2,3-di-O-benzyl-α-D-arabinofuranoside 
• 1431370-59-0 pent-4-enyl 2,3-di-O-benzyl-5-O-(3,5-di-O-benzyl-β-D-arabinofuranosyl)-α-D-arabinofuranoside 
• 1431370-74-9 C₄₃H₄₈O₉ 
• 1431370-55-6 pent-4-enyl 2,3-di-O-benzyl-5-O-(3,5-di-O-benzyl-β-D-ribofuranosyl)-α-D-arabinofuranoside 
• 1431370-50-1 pent-4-enyl 2,3-di-O-benzyl-5-O-(2-O-benzoyl-3,5-di-O-benzyl-β-D-ribofuranosyl)-α-D-arabinofuranoside 

Relevant academic research and scientific papers

Facile synthesis of β- And α-arabinofuranosides and application to cell wall motifs of M. tuberculosis

Propargyl 1,2-orthoesters of arabinose are exploited for the synthesis of 1,2-trans furanosides; easily accessible 1,2-trans ribofuranosides are converted to challenging 1,2-cis-arabinofuranosides by oxidoreduction. Utility of these protocols was demonstrated by the successful synthesis of major structural motifs present in the cell surface of Mycobacterium tuberculosis. Key furanosylations were carried out under gold-catalyzed glycosidation conditions.