Technology Process of (5E,7E,13Z)-(9S,10S)-2-Benzenesulfonyl-10-methoxy-5,9,13-trimethyl-15-(2-trimethylsilanyl-ethoxymethoxy)-cycloheptadeca-5,7,13-triene-1,4-dione
There total 9 articles about (5E,7E,13Z)-(9S,10S)-2-Benzenesulfonyl-10-methoxy-5,9,13-trimethyl-15-(2-trimethylsilanyl-ethoxymethoxy)-cycloheptadeca-5,7,13-triene-1,4-dione which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
caesium carbonate;
In
acetonitrile;
at 45 ℃;
for 3h;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 87 percent / 1.) butyllithium / tetrahydrofuran; hexane / 1.) 0 deg C, 30 min; 2.) -78 deg C, 1 h
2: 85 percent / Dess-Martin periodinane / CH2Cl2 / 1 h
3: 72 percent / cesium carbonate / acetonitrile / 3 h / 45 °C
With
n-butyllithium; caesium carbonate; Dess-Martin periodane;
In
tetrahydrofuran; hexane; dichloromethane; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 100 percent / diisopropylamine, tetrabutylammonium iodide / CH2Cl2 / 2 h / Heating
2: 86 percent / tetrabutylammonium fluoride / tetrahydrofuran / 3 h
3: 88 percent / molecular sieves 4 Angstroem, 1-methylmorpholine-1-oxide, tetrapropylammonium perruthenate / CH2Cl2 / 0.5 h
4: 87 percent / 1.) butyllithium / tetrahydrofuran; hexane / 1.) 0 deg C, 30 min; 2.) -78 deg C, 1 h
5: 85 percent / Dess-Martin periodinane / CH2Cl2 / 1 h
6: 72 percent / cesium carbonate / acetonitrile / 3 h / 45 °C
With
n-butyllithium; tetrapropylammonium perruthennate; 4 A molecular sieve; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; caesium carbonate; Dess-Martin periodane; 4-methylmorpholine N-oxide; diisopropylamine;
In
tetrahydrofuran; hexane; dichloromethane; acetonitrile;