phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-deoxy-1-thio-α-D-mannopyranoside-S-oxide

Base Information

Chemical Name:phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-deoxy-1-thio-α-D-mannopyranoside-S-oxide
CAS No.:1607836-53-2
Molecular Formula:C₄₁H₄₂O₇S
Molecular Weight:678.846
Hs Code.:

Synonyms:phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-deoxy-1-thio-α-D-mannopyranoside-S-oxide

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Chemical Property of phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-deoxy-1-thio-α-D-mannopyranoside-S-oxide

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Technology Process of phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-deoxy-1-thio-α-D-mannopyranoside-S-oxide

There total 4 articles about phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-deoxy-1-thio-α-D-mannopyranoside-S-oxide 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:

: 138181-67-6,127299-78-9
phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside

: 1607836-53-2
phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-deoxy-1-thio-α-D-mannopyranoside-S-oxide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium methylate; methanol / Inert atmosphere

2: sodium hydride; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 0 - 20 °C / Inert atmosphere

3: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 1.5 h / -78 - 20 °C / Inert atmosphere

With methanol; sodium methylate; tetra-(n-butyl)ammonium iodide; sodium hydride; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2014.03.099

Reference yield:

: 127299-77-8
phenyl 3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside

: 1607836-53-2
phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-deoxy-1-thio-α-D-mannopyranoside-S-oxide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 0 - 20 °C / Inert atmosphere

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 1.5 h / -78 - 20 °C / Inert atmosphere

With tetra-(n-butyl)ammonium iodide; sodium hydride; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2014.03.099

Reference yield:

: 108-98-5
thiophenol

: 1607836-53-2
phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-deoxy-1-thio-α-D-mannopyranoside-S-oxide

Guidance literature:: Multi-step reaction with 4 steps

1: boron trifluoride diethyl etherate / Inert atmosphere

2: sodium methylate; methanol / Inert atmosphere

3: sodium hydride; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 0 - 20 °C / Inert atmosphere

4: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 1.5 h / -78 - 20 °C / Inert atmosphere

With methanol; boron trifluoride diethyl etherate; sodium methylate; tetra-(n-butyl)ammonium iodide; sodium hydride; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2014.03.099