351060-19-0

Upstream product

• 154125-79-8 methyl β-xylopyranosyl-(1→4)-β-D-mannopyranoside 
• 159407-17-7 phenyl 2,3-di-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside 
• 351060-18-9 methyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-β-D-mannopyranoside 

Downstream Products

• 351060-20-3 methyl 2,3,6-tri-O-benzyl-β-D-mannopyranoside 
• 351060-23-6 methyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-β-D-mannopyranosyl-(1-3)-2-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl-(1-4)-2,3,6-tri-O-benzyl-β-D-mannopyranoside 
• 351060-25-8 methyl 2,3,6-tri-O-benzyl-β-D-mannopyranosyl-(1-3)-2-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl-(1-4)-2,3,6-tri-O-benzyl-β-D-mannopyranoside 
• 351060-24-7 methyl 2,3-di-O-benzyl-β-D-mannopyranosyl-(1-3)-2-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl-(1-4)-2,3,6-tri-O-benzyl-β-D-mannopyranoside 
• 351060-21-4 methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside 
• 351060-22-5 methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl)-β-D-mannopyranoside 
• 808741-17-5 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl-(1->4)-2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl-(1->4)-2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranoside 
• 808741-20-0 methyl 2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl-(1->4)-2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl-(1->4)-2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranoside 
• 808741-19-7 methyl 2,3-di-O-benzyl-β-D-mannopyranosyl-(1->4)-2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl-(1->4)-2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranoside 
• 808741-16-4 methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-β-D-mannopyranoside 
• 808741-13-1 methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-4,6-benzylidene-β-D-mannopyranosyl)-β-D-mannopyranoside 
• 808741-15-3 methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-β-D-mannopyranosyl)-β-D-mannopyranoside 
• 937023-79-5 C₅₅H₅₆O₁₃ 
• 937023-77-3 C₄₁H₄₈O₁₁ 

Relevant academic research and scientific papers

Synthesis of β-1,4-di-d-mannuronic acid glycosides as potential ligands for toll-like receptors

Toll-like receptors (TLRs) play important roles in host immune defense, and synthetic TLR ligands are useful therapeutic agents for a variety of diseases including infection, inflammation, and cancers. Alginates are strong immune stimulants mediated by TL

Direct chemical synthesis of the β-D-mannans: The β-(1→2) and β-(1→4) series

The direct syntheses of β-(1→2)-mannooctaose and of β-(1→4)-mannohexaose are reported by means of 4,6-O-benzylidene- protected β-mannosyl donors. The synthesis of the (1→2)-mannan was achieved by means of the sulfoxide coupling protocol, whereas the (1→4)

Direct chemical synthesis of the β-mannans: Linear and block syntheses of the alternating β-(1→3)-β-(1→4)-mannan common to Rhodotorula glutinis, Rhodotorula mucilaginosa, and Leptospira biflexa

Two stereocontrolled syntheses of a methyl glycoside of an alternating β-(1→4)-β-(1→3)-mannohexaose, representative of the mannan from Rhodotorula glutinis, Rhodotorula mucilaginosa, and Leptospira biflexa, are described. Both syntheses employ a combinati