Technology Process of C19H32O2Si
There total 10 articles about C19H32O2Si which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 6 steps
1: oxygen; palladium diacetate / dimethyl sulfoxide / 72 h / 55 °C
2: sodium tetrahydroborate; cerium(III) chloride heptahydrate / methanol / 0.25 h
3: tetra-(n-butyl)ammonium iodide; sodium hydride / N,N,N,N,N,N-hexamethylphosphoric triamide / 3 h / -15 °C
4: diisobutylaluminium hydride / dichloromethane / 1 h / 0 °C
5: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / tetrahydrofuran; dimethyl sulfoxide
6: potassium carbonate / methanol / 6 h
With
sodium tetrahydroborate; cerium(III) chloride heptahydrate; oxygen; palladium diacetate; tetra-(n-butyl)ammonium iodide; sodium hydride; diisobutylaluminium hydride; potassium carbonate; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane; dimethyl sulfoxide;
2: Luche reduction / 6: Ohira-Bestmann reaction;
DOI:10.1016/j.tetlet.2011.12.015
- Guidance literature:
-
Multi-step reaction with 4 steps
1: tetra-(n-butyl)ammonium iodide; sodium hydride / N,N,N,N,N,N-hexamethylphosphoric triamide / 3 h / -15 °C
2: diisobutylaluminium hydride / dichloromethane / 1 h / 0 °C
3: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / tetrahydrofuran; dimethyl sulfoxide
4: potassium carbonate / methanol / 6 h
With
tetra-(n-butyl)ammonium iodide; sodium hydride; diisobutylaluminium hydride; potassium carbonate; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane; dimethyl sulfoxide;
4: Ohira-Bestmann reaction;
DOI:10.1016/j.tetlet.2011.12.015
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / tetrahydrofuran; dimethyl sulfoxide
2: potassium carbonate / methanol / 6 h
With
potassium carbonate; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione;
In
tetrahydrofuran; methanol; dimethyl sulfoxide;
2: Ohira-Bestmann reaction;
DOI:10.1016/j.tetlet.2011.12.015