Technology Process of C19H26O7S
There total 2 articles about C19H26O7S which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
(2S,2'R,5'S)-5'-((R)-1,2-Dihydroxy-ethyl)-2,5'-dimethyl-tetrahydro-[2,2']bifuranyl-5-one;
With
di(n-butyl)tin oxide;
In
benzene;
for 3h;
Reflux;
p-toluenesulfonyl chloride;
With
tetrabutylammomium bromide;
In
benzene;
at 20 ℃;
for 0.5h;
DOI:10.1055/s-0030-1258327
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: sodium tetrahydroborate; dimethylsulfide borane complex / tetrahydrofuran; toluene / 2 h / -10 °C
2.1: di(n-butyl)tin oxide / benzene / 3 h / Reflux
2.2: 0.5 h / 20 °C
With
sodium tetrahydroborate; dimethylsulfide borane complex; di(n-butyl)tin oxide;
In
tetrahydrofuran; toluene; benzene;
DOI:10.1055/s-0030-1258327
- Guidance literature:
-
Multi-step reaction with 5 steps
1: tri-n-butyl-tin hydride; sodium iodide; 1,1'-azobis(1-cyanocyclohexanenitrile) / 1,2-dimethoxyethane / 18 h / 80 °C
2: dmap; triethylamine / dichloromethane / 72 h / Reflux
3: diisobutylaluminium hydride / toluene / 2 h / -78 °C
4: calcium chloride / dichloromethane / 18 h / 20 °C
5: ethylaluminum dichloride; diethylaluminium chloride / hexane; dichloromethane / 0.5 h / -78 - -30 °C
With
dmap; tri-n-butyl-tin hydride; ethylaluminum dichloride; diethylaluminium chloride; diisobutylaluminium hydride; triethylamine; sodium iodide; calcium chloride; 1,1'-azobis(1-cyanocyclohexanenitrile);
In
1,2-dimethoxyethane; hexane; dichloromethane; toluene;
DOI:10.1055/s-0030-1258327