Technology Process of C28H50O2Si2
There total 11 articles about C28H50O2Si2 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
tris(acetonitrile)pentamethylcyclopentadienylruthenium(II) hexafluorophosphate;
diastereoselective reaction;
Inert atmosphere;
DOI:10.1021/jacs.6b05127
- Guidance literature:
-
With
tris(acetonitrile)pentamethylcyclopentadienylruthenium(II) hexafluorophosphate;
In
acetone;
at -78 - -5 ℃;
for 12.1h;
Overall yield = 86 %; Overall yield = 2.51 g; diastereoselective reaction;
Inert atmosphere;
DOI:10.1021/ja411270d
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 2,6-dimethylpyridine / Inert atmosphere
2: isopropylmagnesium chloride / Inert atmosphere
3: Inert atmosphere
4: benzo[1,3,2]dioxaborole; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole / 4 h / -78 °C / Inert atmosphere
5: tris(acetonitrile)pentamethylcyclopentadienylruthenium(II) hexafluorophosphate / Inert atmosphere
With
2,6-dimethylpyridine; tris(acetonitrile)pentamethylcyclopentadienylruthenium(II) hexafluorophosphate; isopropylmagnesium chloride; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole; benzo[1,3,2]dioxaborole;
DOI:10.1021/jacs.6b05127