(+)-(2S,3S,4R)-2-(Benzyloxy)-3-<<4-(benzyloxy)-3-methoxyphenyl>bis(phenylthio)methyl>-4-<3-<oxy>benzoyl>tetrahydrofuran

Base Information

Chemical Name:(+)-(2S,3S,4R)-2-(Benzyloxy)-3-<<4-(benzyloxy)-3-methoxyphenyl>bis(phenylthio)methyl>-4-<3-<oxy>benzoyl>tetrahydrofuran
CAS No.:127974-73-6
Molecular Formula:C₅₃H₅₈O₆S₂Si
Molecular Weight:883.257
Hs Code.:

(+)-(2S,3S,4R)-2-(Benzyloxy)-3-<<4-(benzyloxy)-3-methoxyphenyl>bis(phenylthio)methyl>-4-<3-<<dimethyl(2,3-dimethyl-2-butyl)silyl>oxy>benzoyl>tetrahydrofuran

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Chemical Property of (+)-(2S,3S,4R)-2-(Benzyloxy)-3-<<4-(benzyloxy)-3-methoxyphenyl>bis(phenylthio)methyl>-4-<3-<oxy>benzoyl>tetrahydrofuran

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Technology Process of (+)-(2S,3S,4R)-2-(Benzyloxy)-3-<<4-(benzyloxy)-3-methoxyphenyl>bis(phenylthio)methyl>-4-<3-<oxy>benzoyl>tetrahydrofuran

There total 7 articles about (+)-(2S,3S,4R)-2-(Benzyloxy)-3-<<4-(benzyloxy)-3-methoxyphenyl>bis(phenylthio)methyl>-4-<3-<oxy>benzoyl>tetrahydrofuran 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:

: 2426-87-1
3-methoxy-4-(phenylmethoxy)benzaldehyde

: 127974-73-6
(+)-(2S,3S,4R)-2-(Benzyloxy)-3-<<4-(benzyloxy)-3-methoxyphenyl>bis(phenylthio)methyl>-4-<3-<oxy>benzoyl>tetrahydrofuran

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / tributylphosphine / benzene

2: 1) BuLi / 1) THF, -78 deg C, 2) THF, r. t.

With n-butyllithium; tributylphosphine; In benzene;
DOI:10.1021/jo00301a026

Reference yield:

: 591-20-8
3-Bromophenol

: 127974-73-6
(+)-(2S,3S,4R)-2-(Benzyloxy)-3-<<4-(benzyloxy)-3-methoxyphenyl>bis(phenylthio)methyl>-4-<3-<oxy>benzoyl>tetrahydrofuran

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / imidazole / dimethylformamide / 0.83 h

2: 1) Mg, 1,2-dibromoethane / THF

3: chromium trioxide, pyridine / CH₂Cl₂

4: 1) BuLi / 1) THF, -78 deg C, 2) THF, r. t.

With pyridine; 1H-imidazole; chromium(VI) oxide; n-butyllithium; magnesium; ethylene dibromide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00301a026

Reference yield:

: 123195-64-2
1-Bromo-3-<oxy>benzene

: 127974-73-6
(+)-(2S,3S,4R)-2-(Benzyloxy)-3-<<4-(benzyloxy)-3-methoxyphenyl>bis(phenylthio)methyl>-4-<3-<oxy>benzoyl>tetrahydrofuran

Guidance literature:: Multi-step reaction with 3 steps

1: 1) Mg, 1,2-dibromoethane / THF

2: chromium trioxide, pyridine / CH₂Cl₂

3: 1) BuLi / 1) THF, -78 deg C, 2) THF, r. t.

With pyridine; chromium(VI) oxide; n-butyllithium; magnesium; ethylene dibromide; In dichloromethane;
DOI:10.1021/jo00301a026