Technology Process of C21H38O4Si
There total 9 articles about C21H38O4Si 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
potassium osmate(VI) dihydrate; methanesulfonamide; potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; potassium hexacyanoferrate(III);
In
water; tert-butyl alcohol;
at 0 ℃;
for 36h;
optical yield given as %ee;
DOI:10.1021/ml1002184
- Guidance literature:
-
With
AD-Mix-α;
optical yield given as %ee;
stereoselective reaction;
DOI:10.1021/jo201319b
- Guidance literature:
-
Multi-step reaction with 4 steps
1: toluene / 36 h / Reflux
2: lithium aluminium tetrahydride / diethyl ether / 0.17 h / 0 °C / Inert atmosphere
3: 1H-imidazole / N,N-dimethyl-formamide / 16 h / Inert atmosphere
4: potassium osmate(VI) dihydrate; methanesulfonamide; potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; potassium hexacyanoferrate(III) / water; tert-butyl alcohol / 36 h / 0 °C
With
1H-imidazole; potassium osmate(VI) dihydrate; lithium aluminium tetrahydride; methanesulfonamide; potassium carbonate; 1,4-bis(9-O-dihydroquinidine)phthalazine; potassium hexacyanoferrate(III);
In
diethyl ether; water; N,N-dimethyl-formamide; toluene; tert-butyl alcohol;
1: Johnson-Claisen orthoester rearrangement / 4: Sharpless dihydroxylation;
DOI:10.1021/ml1002184