175289-49-3

Upstream product

• 955943-31-4 1’,6,6’-tri-O-tert-butyldimethylsilyl-2,3,3’,4,4’-penta-O-benzylsucrose 
• 63734-13-4 1’,6,6’-tri-O-tert-butyldimethylsilylsucrose 

Downstream Products

• 175289-51-7 2,3,3',4,4'-penta-O-benzyl-6,6'-di-p-nitrobenzoylsucrose 
• 955943-28-9 tri-tert-butyl 2,3,4,3',4'-penta-O-benzyl sucrose tricarboxylate 
• 1326706-59-5 6'-O-(tert-butyldiphenyl)silyl-2,3,3',4,4'-penta-O-benzylsucrose 
• 1326706-67-5 1',6-di-O-acetyl-6'-O-mesyl-2,3,3',4,4'-penta-O-benzylsucrose 
• 1326706-70-0 C₄₇H₅₀O₁₀ 
• 1326706-71-1 6'-deoxy-6'-diphenylphosphinoxide-2,3,3',4,4'-penta-O-benzylsucrose 
• 1326706-60-8 1',6-di-O-acetyl-6'-O-(tert-butyldiphenyl)silyl-2,3,3',4,4'-penta-O-benzylsucrose 
• 1326706-61-9 1',6-di-O-acetyl-2,3,3',4,4'-penta-O-benzylsucrose 

Relevant academic research and scientific papers

Synthesis of Cyclotriveratrylene-Sucrose-Based Capsules

Cyclotriveratrylene (CTV) is a C3-symmetrical macrocycle, which can be used as a chiral building block in the construction of supramolecular containers. Coupling of the CTV unit with a sucrose molecule gave enantiopure water-soluble (after depr

Preparation of 6,6,1′,1′,6′,6′-hexadeutero sucrose

The preparation of 6,6,1′,1′,6′,6′-hexadeutero sucrose is reported. The synthesis is based on a triple oxidation of a protected sucrose 6,1′,6′-triol to the corresponding 6,1′,6′-tricarboxylic acid or ester, followed by reduction with lithium aluminium de