4-[(1-methylimidazoliumhexafluorophospho)methyl]benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside

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Chemical Name:4-[(1-methylimidazoliumhexafluorophospho)methyl]benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside
CAS No.:1312424-05-7
Molecular Formula:C₆₈H₇₃N₂O₁₂*F₆P
Molecular Weight:1255.3
Hs Code.:

4-[(1-methylimidazoliumhexafluorophospho)methyl]benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside

Synonyms:4-[(1-methylimidazoliumhexafluorophospho)methyl]benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside

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Chemical Property of 4-[(1-methylimidazoliumhexafluorophospho)methyl]benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside

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Technology Process of 4-[(1-methylimidazoliumhexafluorophospho)methyl]benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside

There total 1 articles about 4-[(1-methylimidazoliumhexafluorophospho)methyl]benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside 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: 86.8%

: 1312423-97-4
C₃₉H₄₃N₂O₆⁽¹⁺⁾*F₆P^(1-)

: 108869-64-3,130177-78-5,129163-12-8
2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl trichloroacetimidate

: 1312424-05-7
4-[(1-methylimidazoliumhexafluorophospho)methyl]benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 0 ℃; for 0.5h; stereospecific reaction; Molecular sieve; Inert atmosphere;
DOI:10.1021/jo2006126