Technology Process of C32H43NO5SSi
There total 8 articles about C32H43NO5SSi which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
di-isopropyl azodicarboxylate; triphenylphosphine;
In
dichloromethane;
at 0 - 20 ℃;
Inert atmosphere;
DOI:10.1021/jo202054g
- Guidance literature:
-
Multi-step reaction with 6 steps
1: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran; mineral oil / 20 °C / Inert atmosphere
2: lithium aluminium tetrahydride / tetrahydrofuran / -78 - 0 °C / Inert atmosphere
3: triethylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere
4: hydrogenchloride; water / methanol / 40 °C
5: dmap; triethylamine / dichloromethane / 1 h / 0 °C / Inert atmosphere
6: di-isopropyl azodicarboxylate; triphenylphosphine / dichloromethane / 0 - 20 °C / Inert atmosphere
With
hydrogenchloride; dmap; lithium aluminium tetrahydride; di-isopropyl azodicarboxylate; water; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; triphenylphosphine;
In
tetrahydrofuran; methanol; dichloromethane; mineral oil;
6: Mitsunobu reaction;
DOI:10.1021/jo202054g
- Guidance literature:
-
Multi-step reaction with 4 steps
1: triethylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere
2: hydrogenchloride; water / methanol / 40 °C
3: dmap; triethylamine / dichloromethane / 1 h / 0 °C / Inert atmosphere
4: di-isopropyl azodicarboxylate; triphenylphosphine / dichloromethane / 0 - 20 °C / Inert atmosphere
With
hydrogenchloride; dmap; di-isopropyl azodicarboxylate; water; triethylamine; triphenylphosphine;
In
methanol; dichloromethane;
4: Mitsunobu reaction;
DOI:10.1021/jo202054g