Technology Process of Cyclohexanone, 3-(2-methylphenyl)-, (3S)-
There total 10 articles about Cyclohexanone, 3-(2-methylphenyl)-, (3S)- 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
chlorobis(ethylene)rhodium(I) dimer; (R)-(+)-[(η5-1-bis(3,5-dimethylphenyl)phosphino-2-(3-diphenylphosphino-2-methylpropenyl)cyclopentadienyl-P)]manganese(I) dicarbonyl; potassium hydroxide;
In
1,4-dioxane; water;
at 50 ℃;
for 7h;
enantioselective reaction;
Inert atmosphere;
DOI:10.1021/jacs.6b11243
- Guidance literature:
-
With
chlorobis(ethylene)rhodium(I) dimer; ((η5-1-bis-(3,5-dimethylphenyl)phosphino-2-(3-diphenylphosphino-2-methylpropenyl)cyclopentadienyl-p))manganese(I) dicarbonyl; potassium hydroxide;
In
1,4-dioxane;
at 20 - 50 ℃;
for 10h;
Inert atmosphere;
- Guidance literature:
-
trifluoro(2-tolyl)silane;
With
tris(dimethylamino)sulfonium trimethylsilyldifluoride;
In
dichloromethane;
for 0.0833333h;
Inert atmosphere;
cyclohexenone;
With
C41H42BrCuN2;
In
dichloromethane;
at 40 ℃;
for 40h;
Inert atmosphere;
With
hydrogenchloride; water;
In
dichloromethane;
optical yield given as %ee;
enantioselective reaction;
DOI:10.1021/jo900589x