878270-46-3

Upstream product

• 65556-30-1 1,6-di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranoside 

Downstream Products

• 945033-08-9 1-deutero-6-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose 
• 874906-04-4 2,3,4-tri-O-benzyl-1-C-methyl-α-D-mannopyranose 
• 945033-20-5 C₂₉H₂₇⁽²⁾H₄O₆I 
• 945033-11-4 C₃₁H₂₇⁽²⁾H₇O₈ 
• 945033-09-0 1-deutero-2,3,4-tri-O-benzyl-α-D-mannopyranose 

Relevant academic research and scientific papers

Mechanistic studies on the stereoselective formation of β-mannosides from mannosyl iodides using α-deuterium kinetic isotope effects

(Chemical Equation Presented) Stereoselective synthesis of β-mannosides is one of the most challenging linkages to achieve in carbohydrate chemistry. Both the anomeric effect and the C2 axial substituent favor the formation of the axial glycoside (α-produ

Trifluoromethanesulfonic acid efficiently catalyzed the intramolecular glycosidation of 1-C-alkyl-D-hexopyranoses to form the anhydroketopyranoses having 6,8-dioxabicyclo[3.2.1]octane structures

The intramolecular glycosidation of the 1-C-alkyl-D-hexopyranose derivatives to form the anhydroketopyranoses having 6,8-dioxabicyclo[3.2.1] octane structures was investigated. We synthesized several 1-C-alkyl-2,3,4-tri- O-benzyl-D-hexopyranoses and found