106734-69-4

Upstream product

• 582-52-5 1,2:5,6-diacetone-D-glucose 
• 101475-83-6 3-O-benzyl-1,2;5,6-di-O-isopropylidene-α-D-glucofuranoside 
• 76-83-5 trityl chloride 
• 42926-89-6 1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 10368-86-2 1,2:5,6-di-O-isopropylidene-α-D-galactofuranose 
• 65451-98-1 3-O-benzyl-1,2:5,6-di-O-isopropylidene-α-D-galactofuranose 
• 100-44-7 benzyl chloride 

Downstream Products

• 161747-23-5 3-O-benzyl-1,2-O-isopropylidene-5-O-methyl-α-D-galactofuranose 
• 161747-25-7 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-5,7-di-O-methyl-α-D-galacto-hept-6-enofuranose 
• 106734-70-7 3-O-benzyl-1,2-O-isopropylidene-6-O-(triphenylmethyl)-β-L-arabino-hexofuranos-5-ulose 
• 161747-22-4 3-O-benzyl-1,2-O-isopropylidene-5-O-methyl-6-O-trityl-α-D-galactofuranose 

Relevant academic research and scientific papers

Synthesis of carbohydrate fused chiral macrocyclic benzolactones through Sonogashira reaction

Synthesis of 10-, 11- and 12-membered chiral benzolactones fused to furanose/pyranose sugars has been achieved in good to excellent yields using an intramolecular Sonogashira reaction. Positions 1-2, 3-5, 3-6 and 5-6 of sugar were utilized for the constru