p-methoxyphenyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→3)-(4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl)-(1→2)-(4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

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Chemical Name:p-methoxyphenyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→3)-(4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl)-(1→2)-(4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside
CAS No.:1607433-82-8
Molecular Formula:C₉₆H₉₈O₂₃
Molecular Weight:1619.82
Hs Code.:

p-methoxyphenyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→3)-(4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl)-(1→2)-(4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

Synonyms:p-methoxyphenyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→3)-(4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl)-(1→2)-(4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

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Chemical Property of p-methoxyphenyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→3)-(4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl)-(1→2)-(4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

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Technology Process of p-methoxyphenyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→3)-(4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl)-(1→2)-(4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

There total 1 articles about p-methoxyphenyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→3)-(4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl)-(1→2)-(4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside 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: 78.0%

: 1607433-78-2
p-Tolyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→ 3)-4-O-benzoyl-2-O-benzyl-1-thio-β-L-fucopyranoside

: 1607433-81-7
p-methoxyphenyl (4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

: 1607433-82-8
p-methoxyphenyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→3)-(4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl)-(1→2)-(4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside

Guidance literature:: p-Tolyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→ 3)-4-O-benzoyl-2-O-benzyl-1-thio-β-L-fucopyranoside; p-methoxyphenyl (4-O-acetyl-3,6-di-O-benzyl-α-D-galactopyranosyl)-(1→3)-4-O-benzoyl-2-O-benzyl-α-L-fucopyranoside; In diethyl ether; dichloromethane; at 20 ℃; for 1h; Molecular sieve;

With N-iodo-succinimide; silver trifluoromethanesulfonate; In diethyl ether; dichloromethane; at -10 ℃; for 3h; Inert atmosphere;
DOI:10.1021/jo500503r