853308-49-3

Upstream product

• 107-19-7 propargyl alcohol 
• 165877-99-6 2,3,4,6-tetra-O-Bz-β-D-glucopyranosyl bromide 
• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 

Downstream Products

• 128503-39-9 methyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl)-α-D-glucopyranoside 
• 1079963-74-8 C₄₇H₄₆O₁₅ 
• 1079963-70-4 C₅₈H₅₄O₁₅ 
• 1079963-60-2 C₄₅H₄₂O₁₄ 
• 1079963-59-9 C₆₄H₅₈O₁₅ 
• 1079963-58-8 C₆₄H₅₈O₁₅ 
• 1079963-56-6 C₆₄H₅₈O₁₅ 
• 1198083-90-7 C₆₆H₆₄O₁₅ 
• 1198083-87-2 C₆₆H₆₄O₁₅ 
• 1198083-89-4 C₆₆H₆₄O₁₅ 
• 1332305-28-8 N-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyloxycarbonyl)dodecylamine 
• 1332305-26-6 N-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyloxycarbonyl)-1-adamantylamine 
• 1332305-29-9 N-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyloxycarbonyl)-2-(3,4-dimethoxyphenyl)ethylamine 
• 1332305-12-0 methyl N-(9-fluorenylmethoxycarbonyl)-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-L-threoninate 

Relevant academic research and scientific papers

Efficient synthesis of oligosaccharyl 1,2-O-orthoesters from n-pentenyl glycosides and application to the pentaarabinofuranoside of the mycobacterial cell surface

Complex oligosaccharide syntheses employ the use of more than one glycosyl donor and hence, methods for the interconversion of glycosyl donors are highly valuable for the overall synthesis plan. Herein, n-pentenyl glycosides are efficiently converted to g

Gold mediated glycosylations: Selective activation of propargyl 1,2-orthoesters in the presence of aglycones containing a propargyl moiety

Selective activation of propargyl 1,2-orthoesters in the presence of propargyl glycosides and propargyl ethers was studied; a catalytic amount of AuBr3 activated the propargyloxy group of the 1,2-orthoester thereby giving access to disaccharide

Ionic liquid [bmim]PF6-mediated synthesis of 1,2-orthoesters of carbohydrates and the glycosidation reactions of 4-pentenyl orthoesters

A facile synthesis of the 1,2-orthoesters of carbohydrates in the ionic liquid [bmim]PF6 without a quaternary ammonium salt like tetrabutylammonium iodide, is described. The glycosidation reactions of 4-pentenyl orthoesters (NPOEs) with differe

A facile and eco-friendly method for the synthesis of 1,2-orthoesters of carbohydrates in ionic liquid

A facile method for the synthesis of 1,2-orthoesters of carbohydrates in ionic liquid [bmim]PF6 is described. The method described herein is simpler, eco-friendly and avoids the addition of quaternary ammonium salts as promoters.