313468-65-4

Upstream product

• 251451-05-5 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl 2,2,2-trichloroacetimidate 
• 42793-97-5 2,3,5-tri-O-benzoyl-1-O-methyl-α-L-arabinofuranose 
• 134149-34-1 allyl-α-L-arabinofuranoside 
• 98-88-4 benzoyl chloride 
• 251451-10-2 allyl 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->5)-α-L-arabinofuranoside 

Downstream Products

• 251451-11-3 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-α-L-arabinofuranosyl trichloroacetimidate 
• 251451-14-6 allyl 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-α-L-arabinofuranosyl-(1->5)-α-L-arabinofuranosyl-(1->5)-2,3-di-O-benzyl-α-L-arabinofuranoside 
• 251451-16-8 C₆₅H₆₂Cl₃NO₂₆ 
• 251451-18-0 C₆₆H₆₆O₂₆ 

Relevant academic research and scientific papers

An efficient and concise regioselective synthesis of α-(1 → 5)-linked L-arabinofuranosyl oligosaccharides

A series of α-(1 → 5)-linked L-arabinofuranosyl di-, tetra-, hexa- and octameric derivatives were synthesized efficiently. The process was carried out in a regio- and stereoselective manner using perbenzoylated arabinofuranosyl trichloroacetimidates as glycosyl donors and unprotected or partially protected arabinofuranosides as glycosyl acceptors in the presence of a catalytic amount of trimethylsilyl trifluoromethanesulfonate (TMSOTf). (C) 2000 Elsevier Science Ltd.

Regio- and stereoselective synthesis of 1→5-linked α-L- arabinofuranosyl oligosaccharides

Regio- and stereoselective synthesis of furanosyl oligosaccharides in moderate to very good yields using arabinofuranosyl trichloroacetimidates as glycosyl donors and unprotected or partially protected glycosides as acceptors was described. A convergent synthesis of 1→5-linked α-L- arabinofuranosyl octamer was presented.