Technology Process of C28H36O8S2
There total 6 articles about C28H36O8S2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
C19H26O6S;
With
triethylamine;
In
dichloromethane;
at 0 ℃;
for 0.166667h;
2-mesitylenesulphonyl chloride;
With
dmap;
In
dichloromethane;
at 20 ℃;
for 8h;
DOI:10.1021/ol303272w
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: lithium diisopropyl amide / tetrahydrofuran; hexane / 0.33 h / -78 °C
1.2: 21 h / 20 °C
2.1: Hoveyda-Grubbs catalyst second generation / dichloromethane / 36 h
3.1: (S)-N-( p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide / ethanol; 1,2-dichloro-ethane / 0.17 h / 0 °C
3.2: 120 h / 4 °C
4.1: hydrogenchloride / 1,4-dioxane; water / 8 h / 20 °C
5.1: triethylamine / dichloromethane / 0.17 h / 0 °C
5.2: 8 h / 20 °C
With
hydrogenchloride; Hoveyda-Grubbs catalyst second generation; (S)-N-( p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide; triethylamine; lithium diisopropyl amide;
In
tetrahydrofuran; 1,4-dioxane; ethanol; hexane; dichloromethane; water; 1,2-dichloro-ethane;
DOI:10.1021/ol303272w
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: toluene-4-sulfonic acid / dichloromethane / 14 h / 20 °C
2.1: lithium diisopropyl amide / tetrahydrofuran; hexane / 0.33 h / -78 °C
2.2: 21 h / 20 °C
3.1: Hoveyda-Grubbs catalyst second generation / dichloromethane / 36 h
4.1: (S)-N-( p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide / ethanol; 1,2-dichloro-ethane / 0.17 h / 0 °C
4.2: 120 h / 4 °C
5.1: hydrogenchloride / 1,4-dioxane; water / 8 h / 20 °C
6.1: triethylamine / dichloromethane / 0.17 h / 0 °C
6.2: 8 h / 20 °C
With
hydrogenchloride; Hoveyda-Grubbs catalyst second generation; (S)-N-( p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide; toluene-4-sulfonic acid; triethylamine; lithium diisopropyl amide;
In
tetrahydrofuran; 1,4-dioxane; ethanol; hexane; dichloromethane; water; 1,2-dichloro-ethane;
DOI:10.1021/ol303272w