methyl 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside

Base Information

Chemical Name:methyl 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside
CAS No.:1239914-94-3
Molecular Formula:C₁₄₅H₁₅₀O₃₃
Molecular Weight:2420.77
Hs Code.:

methyl 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside

Synonyms:methyl 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside

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Chemical Property of methyl 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside

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Technology Process of methyl 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside

There total 1 articles about methyl 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 73.0%

: 1239914-93-2
4-methylphenyl 2-O-benzoyl-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside

: 1239914-92-1
methyl 2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside

: 1239914-94-3
methyl 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->5)-2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside

Guidance literature:: 4-methylphenyl 2-O-benzoyl-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside; methyl 2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[2,3-O-xylylene-β-D-arabinofuranosyl-(1->2)-3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside; In dichloromethane; at 20 ℃; for 1h; Molecular sieve; Inert atmosphere;

With N-iodo-succinimide; silver trifluoromethanesulfonate; In dichloromethane; at -30 ℃; for 1h; stereoselective reaction; Inert atmosphere;
DOI:10.1021/ol101520q