65236-82-0

Upstream product

• 14218-11-2 2,3,4,6-Tetra-O-benzoyl-α-D-mannopyranosyl bromide 
• 67-56-1 methanol 

Downstream Products

• 439-01-0 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl fluoride 
• 6605-40-9 methyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranoside 
• 1391727-71-1 benzyl 6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-2,3,4-tri-O-benzyl-β-D-glucopyranoside 
• 1391727-77-7 pent-4-enyl 3,4-di-O-benzoyl-6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 1391727-78-8 phenyl 6-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-2,3,4-tri-O-methyl-1-thio-α-D-mannopyranoside 
• 627466-98-2 2,3,4,6-tetra-O-benzoyl-α,β-D-mannospyranose 
• 1352278-39-7 (2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 1352427-79-2 (2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-2,3,4,6-tetra-O-benzoyl-β-D-mannopyranoside 
• 869213-53-6 2-O-benzoyl-3,4,6-tetra-O-benzyl-α-D-mannopyranoside 
• 346441-53-0 allyl O-(2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-(1→6)-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Environmentally benign synthesis of sugar orthoesters promoted by anhydrous sodium acetate and ultrasound

A convenient and alternative procedure for the synthesis of sugar orthoesters from glycosyl bromides with anhydrous sodium acetate as base under ultrasound irradiation is described. Various sugar and sugar-sugar orthoesters were prepared in 70%-91% isolat

A facile method for the preparation of sugar orthoesters promoted by anhydrous sodium bicarbonate

A facile and eco-friendly method for the preparation of sugar orthoesters by using anhydrous sodium bicarbonate is described. Various sugar orthoesers, including sugar sugar orthoesters, were synthesized in good-to-excellent yields by the reaction of a pr

Synthesis of a core arabinomannan oligosaccharide of Mycobacterium tuberculosis

The synthesis of a core arabinomannan (AM) oligosaccharide from Mycobacterium tuberculosis has been achieved using a convergent [6 + 6] glycosylation strategy and a defined set of building blocks. Dodecasaccharide 1, containing the key AM structural featu