5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose

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Chemical Name:5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose
CAS No.:518332-46-2
Molecular Formula:C₄₀H₅₀O₁₁
Molecular Weight:706.83
Hs Code.:

Synonyms:5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose

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Chemical Property of 5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose

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Technology Process of 5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose

There total 12 articles about 5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose 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: 93.0%

: 518332-60-0
3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-α-D-glucopyranosyl]-1,2-O-isopropylidene-5-phenyl-α-D-ribofuranose

: 518332-46-2
5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose

Guidance literature:: 3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-α-D-glucopyranosyl]-1,2-O-isopropylidene-5-phenyl-α-D-ribofuranose; With dmap; phenylcarbonochloridothioate; In acetonitrile; at 20 ℃;

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; Heating;
DOI:10.1021/jm060310d

Reference yield: 93.0%

: thiocarbonic acid O-{[6-(8-benzyloxy-5-benzyloxymethyl-2,3-dimethoxy-2,3-dimethyl-hexahydro-pyrano[3,4-b][1,4]dioxin-7-yloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-phenyl-methyl} ester O-phenyl ester

: 518332-46-2
5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In benzene; for 0.5h; Heating;
DOI:10.1021/ol0602710

Reference yield:

: 518332-41-7
2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-1-phenylsulfinyl-β-D-glucopyranoside

: 518332-46-2
5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose

Guidance literature:: Multi-step reaction with 5 steps

1.1: 78 percent / 2,6-di-tert-butyl-4-methylpyridine / diethyl ether / 8 h / -78 °C

2.1: 82 percent / TBAF / tetrahydrofuran / 20 °C

3.1: tetrahydrofuran / 20 °C

4.1: PhOCSCl; DMAP / acetonitrile / 20 °C

4.2: 93 percent / Bu₃SnH; AIBN / toluene / Heating

With dmap; 2,6-di-tert-butyl-4-methylpyridine; tetrabutyl ammonium fluoride; phenylcarbonochloridothioate; In tetrahydrofuran; diethyl ether; acetonitrile; 3.1: Moffatt oxidation / 5.2: Barton deoxygenation;
DOI:10.1021/jm060310d