552865-74-4

Upstream product

• 184033-07-6 benzyl-{O⁴-[O⁴,O⁶-((R)-benzylidene)-β-D-glucopyranosyl]-β-D-glucopyranoside} 
• 108-24-7 acetic anhydride 

Downstream Products

• 552865-76-6 C₄₉H₄₂F₆O₁₈S₂ 
• 552865-80-2 benzyl 2,3,6-tri-O-benzoyl-β-D-mannopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-β-D-mannopyranoside 
• 552865-77-7 C₆₁H₅₂O₁₆ 
• 552865-78-8 benzyl 2,3-di-O-benzoyl-β-D-mannopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-β-D-mannopyranoside 
• 1053638-91-7 Benzoic acid (3aS,4R,6R,7R,7aS)-4-benzyloxy-2-ethoxy-7-((3aS,4S,5aR,8R,9aR,9bS)-2-ethoxy-2,8-diphenyl-hexahydro-[1,3]dioxolo[4',5':4,5]pyrano[3,2-d][1,3]dioxin-4-yloxy)-2-phenyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethyl ester 
• 552865-75-5 benzyl 3-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzoyl-β-D-glucopyranoside 
• 184033-07-6 benzyl-{O⁴-[O⁴,O⁶-((R)-benzylidene)-β-D-glucopyranosyl]-β-D-glucopyranoside} 

Relevant academic research and scientific papers

The chemical synthesis of beta-(1-->4)-linked D-mannobiose and D-mannotriose.

A D-cellobiose derivative was converted to D-mannobiose via simultaneous epimerization at C-2 and C-2'. Subsequent beta-D-glucosylation and epimerization at C-2" gave D-mannotriose.