phenyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3-di-O-acetyl-4-O-benzyl-1-thio-α-D-mannopyranoside

Base Information

Chemical Name:phenyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3-di-O-acetyl-4-O-benzyl-1-thio-α-D-mannopyranoside
CAS No.:1319152-47-0
Molecular Formula:C₅₂H₅₆O₁₃S
Molecular Weight:921.075
Hs Code.:

Synonyms:phenyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3-di-O-acetyl-4-O-benzyl-1-thio-α-D-mannopyranoside

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Chemical Property of phenyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3-di-O-acetyl-4-O-benzyl-1-thio-α-D-mannopyranoside

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Technology Process of phenyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3-di-O-acetyl-4-O-benzyl-1-thio-α-D-mannopyranoside

There total 5 articles about phenyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3-di-O-acetyl-4-O-benzyl-1-thio-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:

: C₄₈H₅₂O₁₁S

: 108-24-7
acetic anhydride

: 1319152-47-0
phenyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3-di-O-acetyl-4-O-benzyl-1-thio-α-D-mannopyranoside

Guidance literature:: With pyridine; at 0 - 20 ℃;
DOI:10.1016/j.carres.2011.05.006

Reference yield:

: 1319152-36-7
phenyl 2,3-di-O-benzoyl-4-O-benzyl-1-thio-α-D-mannopyranoside

: 1319152-47-0
phenyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3-di-O-acetyl-4-O-benzyl-1-thio-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / -40 - 20 °C / Molecular sieve

2: methanol; sodium methylate / 0 - 20 °C

3: pyridine / 0 - 20 °C

With pyridine; methanol; trimethylsilyl trifluoromethanesulfonate; sodium methylate; In dichloromethane;
DOI:10.1016/j.carres.2011.05.006

Reference yield:

: 159407-19-9
phenyl 4,6-O-benzylidene-1-thio-α-D-mannopyranoside

: 1319152-47-0
phenyl (2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3-di-O-acetyl-4-O-benzyl-1-thio-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1.1: pyridine; dmap / 0 - 20 °C

2.1: borane-THF / tetrahydrofuran / 0.08 h / 0 °C

2.2: 0 - 20 °C

3.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / -40 - 20 °C / Molecular sieve

4.1: methanol; sodium methylate / 0 - 20 °C

5.1: pyridine / 0 - 20 °C

With pyridine; methanol; dmap; borane-THF; trimethylsilyl trifluoromethanesulfonate; sodium methylate; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.carres.2011.05.006