180784-06-9

Upstream product

• 180784-01-4 3-O-benzoyl-5,6-O-isopropylidene-1,2-O-<1-(exo-methoxycarbonyl)ethylidene>-α-D-galactofuranose 
• 98-88-4 benzoyl chloride 
• 121018-05-1 (2S,3aR,5R,6S,6aR)-5-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-6-hydroxy-2-methyl-tetrahydro-furo[2,3-d][1,3]dioxole-2-carboxylic acid methyl ester 
• 180784-04-7 3-O-benzoyl-1,2-O-<1-(exo-methoxycarbonyl)ethylidene>-α-D-galactofuranose 

Downstream Products

• 180784-08-1 3,6-di-O-benzoyl-1,2-O-<1-(exo-methoxycarbonyl)ethylidene>-5-O-trityl-α-D-galactofuranose 
• 152876-37-4 3,6-di-O-benzoyl-5-O-trityl-1,2-O-<1-(exo-cyano)ethylidene>-α-D-galactofuranose 

Relevant academic research and scientific papers

Synthesis of (1->5)-β-D-galactofuranan and cyclo5)-β-D-galactofurano>oligosaccharides

Synthesis of a linear (1->5)-β-D-galactofuranan was accomplished by trityl-cyanoethylidene polycondensation.On 10-fold reduction in the monomer concentration, the condensation products are cyclic oligosaccharides; the formation of 1,5-anhydro-α-D-galactofuranose was also demonstrated. - Key words: 3,6-di-O-benzoyl-5-O-trityl-1,2-O--α-D-galactofuranose, polycondensation; (1->5)-β-D-galactofuranan, cyclooligomerization, concentration dependence; cyclooligosaccharides; 1,5-anhydro-α-D-galactofuranose.