1310050-46-4

Upstream product

• 211801-76-2 p-methylphenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-1-thio-α/β-D-galactopyranoside 
• 77-76-9 2,2-dimethoxy-propane 
• 106-45-6 para-thiocresol 
• 84278-00-2 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-D-galactopyranose 

Downstream Products

• 1310050-48-6 C₂₄H₂₇N₃O₆S 
• 1310050-45-3 3,4-di-O-acetyl-2-azido-6-O-benzyl-2-deoxy-α-D-galactopyranose 1-O-trichloroacetimidate 
• 1310050-61-3 C₄₅H₄₅N₃O₁₅ 
• 1310050-47-5 C₂₃H₂₇N₃O₄S 

Relevant academic research and scientific papers

4,6-Di-O-Benzylidenyl group-directed preparation of 2-deoxy-2-azido-α-D-galactopyranosides promoted by 3-O-TBDPS

In this study, we designed a method to prepare 2-deoxy-2-azido-α-D-galactopyranosidic bonds using 4,6-di-O-benzylidenyl-3-O-t-butyldiphenylsilyl protected 2-deoxy-2-azido-1-thio-D-galactopyranoside 5 as donors. The donor 5 gives a good to excellent α-sele

Study of the stereoselectivity of 2-azido-2-deoxygalactosyl donors: Remote protecting group effects and temperature dependency

The stereoselectivity of glycosylation reactions is affected by many factors. Synthesis of 1,2-cis glycosidic linkages (such as α linkages in glucose and galactose like monosaccharides) is challenging due to lack of control of the stereoselectivity. Our s