1310050-38-4

Upstream product

• 1310050-37-3 C₂₀H₂₁N₃O₄S 
• 100-39-0 benzyl bromide 
• 125760-23-8 4-methylphenyl 2-azido-4,6-O-benzylidene-2-deoxy-1-thio-β-D-galactopyranoside 
• 100-52-7 benzaldehyde 
• 1125-88-8 benzaldehyde dimethyl acetal 

Downstream Products

• 1310050-39-5 C₂₇H₂₉N₃O₄S 
• 1310050-40-8 C₂₉H₃₁N₃O₅S 
• 130257-35-1 4-O-acetyl-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-galactopyranose 1-O-trichloroacetimidate 
• 1310050-43-1 C₂₇H₂₉N₃O₄S 
• 1310050-44-2 C₂₉H₃₁N₃O₅S 
• 1310050-42-0 6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-α-D-galactopyranose 1-O-trichloroacetimidate 
• 1310050-53-3 C₂₀H₂₃N₃O₄S 
• 1310050-54-4 C₂₄H₂₇N₃O₆S 
• 1310050-52-2 4,6-di-O-acetyl-2-azido-3-O-benzyl-2-deoxy-α-D-galactopyranose 1-O-trichloroacetimidate 
• 1310050-59-9 C₅₀H₄₉N₃O₁₄ 
• 1310050-60-2 C₅₀H₄₉N₃O₁₄ 
• 1310050-63-5 C₄₅H₄₅N₃O₁₅ 

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

Sub-stoichiometric reductive etherification of carbohydrate substrates and one-pot protecting group manipulation

In this study, we report a new reductive etherification procedure for protection of carbohydrate substrates and its application for one-pot preparation of glycosyl building blocks. The reported procedure features the use of polymethylhydrosiloxane (PMHS)

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