3-O-benzyl-5-deoxy-5-C-[benzyl 2,3,4-tri-O-benzyl-7-deoxy-α-D-manno-heptopyranosid-6-ulose-7(E)-ylidene]-1,2-O-isopropylidene-α-D-xylofuranose

Base Information

Chemical Name:3-O-benzyl-5-deoxy-5-C-[benzyl 2,3,4-tri-O-benzyl-7-deoxy-α-D-manno-heptopyranosid-6-ulose-7(E)-ylidene]-1,2-O-isopropylidene-α-D-xylofuranose
CAS No.:253596-64-4
Molecular Formula:C₅₀H₅₂O₁₀
Molecular Weight:812.957
Hs Code.:

Synonyms:3-O-benzyl-5-deoxy-5-C-[benzyl 2,3,4-tri-O-benzyl-7-deoxy-α-D-manno-heptopyranosid-6-ulose-7(E)-ylidene]-1,2-O-isopropylidene-α-D-xylofuranose

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Chemical Property of 3-O-benzyl-5-deoxy-5-C-[benzyl 2,3,4-tri-O-benzyl-7-deoxy-α-D-manno-heptopyranosid-6-ulose-7(E)-ylidene]-1,2-O-isopropylidene-α-D-xylofuranose

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Technology Process of 3-O-benzyl-5-deoxy-5-C-[benzyl 2,3,4-tri-O-benzyl-7-deoxy-α-D-manno-heptopyranosid-6-ulose-7(E)-ylidene]-1,2-O-isopropylidene-α-D-xylofuranose

There total 4 articles about 3-O-benzyl-5-deoxy-5-C-[benzyl 2,3,4-tri-O-benzyl-7-deoxy-α-D-manno-heptopyranosid-6-ulose-7(E)-ylidene]-1,2-O-isopropylidene-α-D-xylofuranose 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: 82.0%

: 23558-05-6
3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose

: 222417-79-0
dimethyl (benzyl 2,3,4-tri-O-benzyl-α-D-manno-heptopyranos-6-ulos-7-yl)phosphonate

: 253596-64-4
3-O-benzyl-5-deoxy-5-C-[benzyl 2,3,4-tri-O-benzyl-7-deoxy-α-D-manno-heptopyranosid-6-ulose-7(E)-ylidene]-1,2-O-isopropylidene-α-D-xylofuranose

Guidance literature:: With 18-crown-6 ether; potassium carbonate; In toluene; at 20 ℃;
DOI:10.1080/07328309908544046

Reference yield:

: 57783-76-3
benzyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside

: 253596-64-4
3-O-benzyl-5-deoxy-5-C-[benzyl 2,3,4-tri-O-benzyl-7-deoxy-α-D-manno-heptopyranosid-6-ulose-7(E)-ylidene]-1,2-O-isopropylidene-α-D-xylofuranose

Guidance literature:: Multi-step reaction with 4 steps

1.1: CrO₃; H₂SO₄

3.1: butyllithium / tetrahydrofuran; hexane / 0.25 h / -78 °C

3.2: 75 percent / tetrahydrofuran; hexane / -78 - 20 °C

4.1: 82 percent / potassium carbonate; 18-crown-6 / toluene / 20 °C

With chromium(VI) oxide; n-butyllithium; 18-crown-6 ether; sulfuric acid; potassium carbonate; In tetrahydrofuran; hexane; toluene; 1.1: Oxidation / 2.1: Methylation / 3.1: Metallation / 3.2: Substitution / 4.1: Substitution;
DOI:10.1080/07328309908544046

Reference yield:

: 253596-63-3
(2S,3S,4S,5S,6S)-3,4,5,6-Tetrakis-benzyloxy-tetrahydro-pyran-2-carboxylic acid methyl ester

: 253596-64-4
3-O-benzyl-5-deoxy-5-C-[benzyl 2,3,4-tri-O-benzyl-7-deoxy-α-D-manno-heptopyranosid-6-ulose-7(E)-ylidene]-1,2-O-isopropylidene-α-D-xylofuranose

Guidance literature:: Multi-step reaction with 2 steps

1.1: butyllithium / tetrahydrofuran; hexane / 0.25 h / -78 °C

1.2: 75 percent / tetrahydrofuran; hexane / -78 - 20 °C

2.1: 82 percent / potassium carbonate; 18-crown-6 / toluene / 20 °C

With n-butyllithium; 18-crown-6 ether; potassium carbonate; In tetrahydrofuran; hexane; toluene; 1.1: Metallation / 1.2: Substitution / 2.1: Substitution;
DOI:10.1080/07328309908544046