Technology Process of (1R,2R,3R,4S,6R)-3-O-acetyl-1,2-di-O-benzyl-6-benzyloxymethyl-4-iodocyclohexane-1,2,3-triol
There total 7 articles about (1R,2R,3R,4S,6R)-3-O-acetyl-1,2-di-O-benzyl-6-benzyloxymethyl-4-iodocyclohexane-1,2,3-triol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
dmap;
In
pyridine; dichloromethane;
for 24h;
Ambient temperature;
DOI:10.1039/P19940002017
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 1.) NaH, 2.) tetrabutylammonium iodide / 1.) THF, 0 deg C, 1 h, 2.) 60 deg C, 12 h
2: 90 percent / aq. TFA / CH2Cl2 / 24 h / Ambient temperature
3: 93 percent / Et3N, thionyl chloride / CH2Cl2 / 0.08 h / 0 °C
4: 89 percent / aq. RuCl3, NaIO4 / CCl4; acetonitrile / 1 h / 0 °C
5: 1.) Bu4NI, 2.) conc. H2SO4 / 1.) THF, reflux, 6 h, 2.) H2O, 60 deg C, 30 min
6: 95 percent / DMAP / pyridine; CH2Cl2 / 24 h / Ambient temperature
With
dmap; ruthenium trichloride; sodium periodate; thionyl chloride; sulfuric acid; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; trifluoroacetic acid;
In
pyridine; tetrachloromethane; dichloromethane; acetonitrile;
DOI:10.1039/P19940002017
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 1.) NaH, 2.) tetrabutylammonium iodide / 1.) THF, 0 deg C, 1 h, 2.) 60 deg C, 12 h
2: 90 percent / aq. TFA / CH2Cl2 / 24 h / Ambient temperature
3: 93 percent / Et3N, thionyl chloride / CH2Cl2 / 0.08 h / 0 °C
4: 89 percent / aq. RuCl3, NaIO4 / CCl4; acetonitrile / 1 h / 0 °C
5: 1.) Bu4NI, 2.) conc. H2SO4 / 1.) THF, reflux, 6 h, 2.) H2O, 60 deg C, 30 min
6: 95 percent / DMAP / pyridine; CH2Cl2 / 24 h / Ambient temperature
With
dmap; ruthenium trichloride; sodium periodate; thionyl chloride; sulfuric acid; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; trifluoroacetic acid;
In
pyridine; tetrachloromethane; dichloromethane; acetonitrile;
DOI:10.1039/P19940002017