2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose

Base Information

Chemical Name:2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose
CAS No.:329973-33-3
Molecular Formula:C₅₄H₄₆O₁₆
Molecular Weight:950.95
Hs Code.:

Synonyms:2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose

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Chemical Property of 2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose

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Technology Process of 2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose

There total 3 articles about 2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose 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: 90.0%

: 329973-31-1
2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-1,2,3,6-tetra-O-benzoyl-α-D-mannopyranose

: 329973-33-3
2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose

Guidance literature:: With dimethyl amine; In tetrahydrofuran; acetonitrile; at 20 ℃;
DOI:10.1039/b004653l

Reference yield:

: 1146468-69-0
2,3,4-Tri-O-benzoyl-6-desoxy-α,β-D-galactopyranose

: 329973-33-3
2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / DBU / CH₂Cl₂ / 2 h / 0 °C

2: 62 percent / TMSOTf; molecular sieves 4 Angstroem / CH₂Cl₂ / 1.5 h / -70 - -10 °C

3: 90 percent / Me₂NH / tetrahydrofuran; acetonitrile / 20 °C

With trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; 1,8-diazabicyclo[5.4.0]undec-7-ene; dimethyl amine; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1039/b004653l

Reference yield:

: 122037-30-3
(2R,3S,4S,5R,6R)-2-methyl-6-(2,2,2-trichloro-1-iminoethoxy)tetrahydro-2H-pyran-3,4,5-triyl tribenzoate

: 329973-33-3
2,3,4-Tri-O-benzoyl-β-D-fucopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-α-D-mannopyranose

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / TMSOTf; molecular sieves 4 Angstroem / CH₂Cl₂ / 1.5 h / -70 - -10 °C

2: 90 percent / Me₂NH / tetrahydrofuran; acetonitrile / 20 °C

With trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; dimethyl amine; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1039/b004653l