methyl 2-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-4-O-(3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

Base Information

Chemical Name:methyl 2-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-4-O-(3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside
CAS No.:158819-00-2
Molecular Formula:C₈₁H₈₀O₁₈
Molecular Weight:1341.52
Hs Code.:

Synonyms:methyl 2-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-4-O-(3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

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Chemical Property of methyl 2-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-4-O-(3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

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Technology Process of methyl 2-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-4-O-(3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

There total 3 articles about methyl 2-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-4-O-(3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 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: 71.0%

: 136824-12-9
methyl 3,4,6-tri-O-benzyl-β-D-mannopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

: 14262-83-0
2,3,4-tri-O-benzoyl-α-D-xylopyranosyl bromide

: 158819-00-2
methyl 2-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-4-O-(3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

Guidance literature:: With silver trifluoromethanesulfonate; In dichloromethane; toluene; at -40 ℃; for 0.5h;
DOI:10.1021/jo00101a036

Reference yield:

: 19488-48-3
methyl O-2,3,6-tri-O-benzyl-α-D-glucopyranoside

: 158819-00-2
methyl 2-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-4-O-(3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) molecular sieves (4 Angstroem), 2.) NaBH₄ / 1.) silver aluminosilicate catalyst / 1.) CH₂Cl₂, r.t., 2.) MeOH, CH₂Cl₂, 0 deg C, 4 h

2: 71 percent / AgOTf / CH₂Cl₂; toluene / 0.5 h / -40 °C

With sodium tetrahydroborate; 4 A molecular sieve; silver trifluoromethanesulfonate; silver aluminosilicate catalyst; In dichloromethane; toluene;
DOI:10.1021/jo00101a036

Reference yield:

: 158818-92-9
3,4,6-tri-O-benzyl-α-D-arabino-hexopyranose-2-ulosyl bromide

: 158819-00-2
methyl 2-O-(2,3,4-tri-O-benzoyl-β-D-xylopyranosyl)-4-O-(3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) molecular sieves (4 Angstroem), 2.) NaBH₄ / 1.) silver aluminosilicate catalyst / 1.) CH₂Cl₂, r.t., 2.) MeOH, CH₂Cl₂, 0 deg C, 4 h

2: 71 percent / AgOTf / CH₂Cl₂; toluene / 0.5 h / -40 °C

With sodium tetrahydroborate; 4 A molecular sieve; silver trifluoromethanesulfonate; silver aluminosilicate catalyst; In dichloromethane; toluene;
DOI:10.1021/jo00101a036