(R)-4-Isopropyl-3-{2-[(1R,2S)-2-(4-methoxy-benzyloxy)-4-methyl-1-triisopropylsilanyloxymethyl-pent-4-enyloxy]-acetyl}-oxazolidin-2-one

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Chemical Name:(R)-4-Isopropyl-3-{2-[(1R,2S)-2-(4-methoxy-benzyloxy)-4-methyl-1-triisopropylsilanyloxymethyl-pent-4-enyloxy]-acetyl}-oxazolidin-2-one
CAS No.:865540-16-5
Molecular Formula:C₃₂H₅₃NO₇Si
Molecular Weight:591.861
Hs Code.:

Synonyms:(R)-4-Isopropyl-3-{2-[(1R,2S)-2-(4-methoxy-benzyloxy)-4-methyl-1-triisopropylsilanyloxymethyl-pent-4-enyloxy]-acetyl}-oxazolidin-2-one

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Chemical Property of (R)-4-Isopropyl-3-{2-[(1R,2S)-2-(4-methoxy-benzyloxy)-4-methyl-1-triisopropylsilanyloxymethyl-pent-4-enyloxy]-acetyl}-oxazolidin-2-one

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Technology Process of (R)-4-Isopropyl-3-{2-[(1R,2S)-2-(4-methoxy-benzyloxy)-4-methyl-1-triisopropylsilanyloxymethyl-pent-4-enyloxy]-acetyl}-oxazolidin-2-one

There total 10 articles about (R)-4-Isopropyl-3-{2-[(1R,2S)-2-(4-methoxy-benzyloxy)-4-methyl-1-triisopropylsilanyloxymethyl-pent-4-enyloxy]-acetyl}-oxazolidin-2-one 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: 90.0%

: C₃₁H₅₂O₇Si

: 95530-58-8
(R)-4-isopropyloxazolidin-2-one

: 865540-16-5
(R)-4-Isopropyl-3-{2-[(1R,2S)-2-(4-methoxy-benzyloxy)-4-methyl-1-triisopropylsilanyloxymethyl-pent-4-enyloxy]-acetyl}-oxazolidin-2-one

Guidance literature:: With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 1h;
DOI:10.1021/ol051543m

Reference yield:

: 865540-35-8
2,7-dimethylocta-1,7-diene-4,5-diol

: 865540-16-5
(R)-4-Isopropyl-3-{2-[(1R,2S)-2-(4-methoxy-benzyloxy)-4-methyl-1-triisopropylsilanyloxymethyl-pent-4-enyloxy]-acetyl}-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 8 steps

1.1: sodium periodate; buffer / CH₂Cl₂ / 0 - 20 °C / pH 4

2.1: TiCl₄; (-)-sparteine / CH₂Cl₂ / 1 h / -78 °C

2.2: CH₂Cl₂ / 0.5 h / -78 °C

2.3: 0.128 g / lithium borohydride / diethyl ether; methanol; tetrahydrofuran / 1 h / 0 °C

3.1: 95 percent / imidazole / dimethylformamide / 15 h / 20 °C

4.1: 86 percent / sodium hydride / dimethylformamide; various solvent(s) / 0 - 20 °C

5.1: 86 percent / Ti(Oi-Pr)4; n-BuMgCl / diethyl ether / 0 °C

6.1: sodium hydride / tetrahydrofuran; various solvent(s) / 0.17 h / 0 °C

6.2: 91 percent / tetrahydrofuran; various solvent(s); dimethylformamide / 0 - 20 °C

7.1: triethylamine / tetrahydrofuran / -78 - 0 °C

8.1: 90 percent / n-BuLi / tetrahydrofuran; hexane / 1 h / -78 °C

With 1H-imidazole; titanium(IV) isopropylate; sodium periodate; n-butyllithium; butyl magnesium bromide; titanium tetrachloride; sodium hydride; triethylamine; (-)-sparteine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol051543m

Reference yield:

: 865540-36-9
(2R,3S)-2-Allyloxy-5-methyl-hex-5-ene-1,3-diol

: 865540-16-5
(R)-4-Isopropyl-3-{2-[(1R,2S)-2-(4-methoxy-benzyloxy)-4-methyl-1-triisopropylsilanyloxymethyl-pent-4-enyloxy]-acetyl}-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: 95 percent / imidazole / dimethylformamide / 15 h / 20 °C

2.1: 86 percent / sodium hydride / dimethylformamide; various solvent(s) / 0 - 20 °C

3.1: 86 percent / Ti(Oi-Pr)4; n-BuMgCl / diethyl ether / 0 °C

4.1: sodium hydride / tetrahydrofuran; various solvent(s) / 0.17 h / 0 °C

4.2: 91 percent / tetrahydrofuran; various solvent(s); dimethylformamide / 0 - 20 °C

5.1: triethylamine / tetrahydrofuran / -78 - 0 °C

6.1: 90 percent / n-BuLi / tetrahydrofuran; hexane / 1 h / -78 °C

With 1H-imidazole; titanium(IV) isopropylate; n-butyllithium; butyl magnesium bromide; sodium hydride; triethylamine; In tetrahydrofuran; diethyl ether; hexane; N,N-dimethyl-formamide;
DOI:10.1021/ol051543m