193953-68-3

Upstream product

• 3947-62-4 2,3,4,5-tetra-O-acetyl-D-glucopyranose 
• 193953-62-7 C₁₀H₂₃N₂O₇P 
• 193953-64-9 C₄₇H₅₃N₂O₁₀PSi 
• 193953-63-8 C₂₆H₄₁N₂O₇PSi 
• 134637-13-1 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl P,P-diphenyl-N-(p-toluenesulfonyl)phosphinimidate 
• 193953-61-6 2,3,4-tri-O-benzoyl-α-D-glucopyranosyl tetramethylphosphoroamidate 
• 98-88-4 benzoyl chloride 
• 143520-19-8 C₃₈H₄₇N₂O₇P 

Relevant academic research and scientific papers

Oligosaccharide synthesis based on glycosyl donors and accepters carrying phosphorus-containing leaving groups

Efficient synthetic strategy for oligosaccharides has been developed by exploiting the difference in anomeric reactivity between glycosyl donors and acceptors carrying phosphorus-containing leaving groups, wherein, the tetramethylphosphoroamidate group plays a pivotal role as anomeric protective group as well as leaving group.